Cblb endonuclease variants, compositions, and methods of use

ABSTRACT

The present disclosure provides improved genome editing compositions and methods for editing a CBLB gene. The disclosure further provides genome edited cells for the prevention, treatment, or amelioration of at least one symptom of, a cancer, an infectious disease, an autoimmune disease, an inflammatory disease, or an immunodeficiency.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of International PCT PatentApplication No. PCT/US2018/054347, which was filed on Oct. 4, 2018, nowpending, which is incorporated by reference herein in its entirety.

STATEMENT REGARDING SEQUENCE LISTING

The Sequence Listing associated with this application is provided intext format in lieu of a paper copy, and is hereby incorporated byreference into the specification. The name of the text file containingthe Sequence Listing is BLBD_087_06US_ST25.txt. The text file is about153 KB, was created on Jan. 14, 2021, and is being submittedelectronically via EFS-Web, concurrent with the filing of thespecification.

BACKGROUND Technical Field

The present disclosure relates to improved genome editing compositions.More particularly, the disclosure relates to nuclease variants,compositions, and methods of using the same for editing the humancasitas B-lineage (Cbl) lymphoma proto-oncogene B (CBLB) gene.

Description of the Related Art

The global burden of cancer doubled between 1975 and 2000. Cancer is thesecond leading cause of morbidity and mortality worldwide, withapproximately 14.1 million new cases and 8.2 million cancer relateddeaths in 2012. The most common cancers are breast cancer, lung andbronchus cancer, prostate cancer, colon and rectum cancer, bladdercancer, melanoma of the skin, non-Hodgkin lymphoma, thyroid cancer,kidney and renal pelvis cancer, endometrial cancer, leukemia, andpancreatic cancer. The number of new cancer cases is projected to riseto 22 million within the next two decades.

The immune system has a key role in detecting and combating humancancer. The majority of transformed cells are quickly detected by immunesentinels and destroyed through the activation of antigen-specific Tcells via clonally expressed T cell receptors (TCR). Accordingly, cancercan be considered an immunological disorder, a failure of immune systemto mount the necessary anti-tumor response to durably suppress andeliminate the disease. In order to more effectively combat cancer,certain immunotherapy interventions developed over the last few decadeshave specifically focused on enhancing T cell immunity. These treatmentshave yielded only sporadic cases of disease remission, and have not hadsubstantial overall success.

Most recently, adoptive cellular therapy strategies, which are based onthe isolation, modification, expansion and reinfusion of T cells, havebeen explored and tested in early stage clinical trials. T cells haveoften been the effector cells of choice for cancer immunotherapy due totheir selective recognition and powerful effector mechanisms. Thesetreatments have shown mixed rates of success, but a small number ofpatients have experienced durable remissions, highlighting the as-yetunrealized potential for T cell-based immunotherapies.

Successful recognition of tumor cell associated antigens by cytolytic Tcells initiates targeted tumor lysis and underpins any effective cancerimmunotherapy approach. Tumor-infiltrating T cells (TILs) express TCRsspecifically directed tumor-associated antigens; however, substantialnumbers of TILs are limited to only a few human cancers. Engineered Tcell receptors (TCRs) and chimeric antigen receptors (CARs) potentiallyincrease the applicability of T cell-based immunotherapy to many cancersand other immune disorders.

In addition, state of the art engineered T cells are still regulated bya complex immunosuppressive tumor microenvironment that consists ofcancer cells, inflammatory cells, stromal cells and cytokines. Amongthese components, cancer cells, inflammatory cells and suppressivecytokines adversely impact T cell phenotype and function. Collectively,the tumor microenvironment drives T cells to terminally differentiateinto exhausted T cells.

T cell exhaustion is a state of T cell dysfunction in a chronicenvironment marked by increased expression of, or increased signaling byinhibitory receptors; reduced effector cytokine production; and adecreased ability to persist and eliminate cancer. Exhausted T cellsalso show loss of function in a hierarchical manner: decreased IL-2production and ex vivo killing capacity are lost at the early stage ofexhaustion, TNF-α production is lost at the intermediate stage, andIFN-γ and GzmB production are lost at the advanced stage of exhaustion.Most T cells in the tumor microenvironment differentiate into exhaustedT cells and lose the ability to eliminate cancer and are eventuallycleared.

To date there have been no demonstrable clinical examples of adoptivecellular therapies with increased persistence and resistance to theimmunosuppressive tumor microenvironment.

BRIEF SUMMARY

The present disclosure generally relates, in part, to compositionscomprising homing endonuclease variants and megaTALs that cleave atarget site in the human casitas B-lineage (Cbl) lymphoma proto-oncogeneB (CBLB) gene and methods of using the same.

In various embodiments, the present disclosure contemplates, in part, apolypeptide comprising a homing endonuclease (HE) variant that cleaves atarget site in the human CBLB gene.

In particular embodiments, the HE variant is an LAGLIDADG homingendonuclease (LHE) variant.

In some embodiments, the polypeptide comprises a biologically activefragment of the HE variant.

In certain embodiments, the biologically active fragment lacks the 1, 2,3, 4, 5, 6, 7, or 8 N-terminal amino acids compared to a correspondingwild type HE.

In some embodiments, the biologically active fragment lacks the 4N-terminal amino acids compared to a corresponding wild type HE.

In further embodiments, the biologically active fragment lacks the 8N-terminal amino acids compared to a corresponding wild type HE.

In particular embodiments, the biologically active fragment lacks the 1,2, 3, 4, 5, or 6 C-terminal amino acids compared to a corresponding wildtype HE.

In particular embodiments, the biologically active fragment lacks theC-terminal amino acid compared to a corresponding wild type HE.

In additional embodiments, the biologically active fragment lacks the 2C-terminal amino acids compared to a corresponding wild type HE.

In particular embodiments, the HE variant is a variant of an LHEselected from the group consisting of: I-CreI and I-SceI.

In certain embodiments, the HE variant is a variant of an LHE selectedfrom the group consisting of: I-AabMI, I-AaeMI, I-AniI, I-ApaMI,I-CapIII, I-CapIV, I-CkaMI, I-CpaMI, I-CpaMII, I-CpaMIII, I-CpaMIV,I-CpaMV, I-CpaV, I-CraMI, I-EjeMI, I-GpeMI, I-GpiI, I-GzeMI, I-GzeMIII,I-HjeMI, I-LtrII, I-LtrI, I-LtrWI, I-MpeMI, I-MveMI, I-Ncrl, I-NcrMI,I-OheMI, I-OnuI, I-OsoMI, I-OsoMIV, I-PanMI, I-PanMII, I-PnoMI, I-ScuMI,I-SmaMI, I-SscMI, and I-Vdi141I.

In some embodiments, the HE variant is a variant of an LHE selected fromthe group consisting of: I-CpaMI, I-HjeMI, I-OnuI, I-PanMI, and SmaMI.

In additional embodiments, the HE variant is an I-OnuI LHE variant.

In particular embodiments, the HE variant comprises one or more aminoacid substitutions in the DNA recognition interface at amino acidpositions selected from the group consisting of: 24, 26, 28, 30, 32, 34,35, 36, 37, 38, 40, 42, 44, 46, 48, 68, 70, 72, 75, 76, 78, 80, 82, 180,182, 184, 186, 188, 189, 190, 191, 192, 193, 195, 197, 199, 201, 203,223, 225, 227, 229, 231, 232, 234, 236, 238, and 240 of an I-OnuI LHEamino acid sequence as set forth in SEQ ID NOs: 1-5, or a biologicallyactive fragment thereof.

In certain embodiments, the HE variant comprises at least 5, at least15, preferably at least 25, more preferably at least 35, or even morepreferably at least 40 or more amino acid substitutions in the DNArecognition interface at amino acid positions selected from the groupconsisting of: 24, 26, 28, 30, 32, 34, 35, 36, 37, 38, 40, 42, 44, 46,48, 68, 70, 72, 75, 76, 78, 80, 82, 180, 182, 184, 186, 188, 189, 190,191, 192, 193, 195, 197, 199, 201, 203, 223, 225, 227, 229, 231, 232,234, 236, 238, and 240 of an I-OnuI LHE amino acid sequence as set forthin SEQ ID NOs: 1-5, or a biologically active fragment thereof.

In particular embodiments, the HE variant comprises one or more aminoacid substitutions at amino acid positions selected from the groupconsisting of: 19, 24, 26, 28, 30, 32, 34, 35, 36, 37, 38, 40, 42, 44,46, 48, 59, 68, 70, 72, 75, 76 77, 78, 80, 82, 168, 180, 182, 184, 186,188, 189, 190, 191, 192, 193, 195, 197, 199, 201, 203, 223, 225, 227,229, 231, 232, 234, 236, 238, and 240 of an I-OnuI LHE amino acidsequence as set forth in SEQ ID NOs: 1-5, or a biologically activefragment thereof.

In certain embodiments, the HE variant comprises at least 5, at least15, preferably at least 25, more preferably at least 35, or even morepreferably at least 40 or more amino acid substitutions at amino acidpositions selected from the group consisting of: 19, 24, 26, 28, 30, 32,34, 35, 36, 37, 38, 40, 42, 44, 46, 48, 59, 68, 70, 72, 75, 76 77, 78,80, 82, 168, 180, 182, 184, 186, 188, 189, 190, 191, 192, 193, 195, 197,199, 201, 203, 223, 225, 227, 229, 231, 232, 234, 236, 238, and 240 ofan I-OnuI LHE amino acid sequence as set forth in SEQ ID NOs: 1-5, or abiologically active fragment thereof.

In particular embodiments, the HE variant comprises at least 5, at least15, preferably at least 25, more preferably at least 35, or even morepreferably at least 40 or more amino acid substitutions in at least oneposition selected from the position group consisting of positions: 24,26, 28, 30, 32, 34, 35, 36, 37, 38, 40, 42, 44, 46, 48, 68, 70, 72, 78,80, 92, 116, 138, 143, 159, 168, 178, 180, 182, 184, 186, 188, 189, 190,191, 192, 193, 195, 197, 199, 201, 203, 207, 223, 225, 227, 232, 236,and 238 of any one of SEQ ID NOs: 1-5, or a biologically active fragmentthereof.

In some embodiments, the HE variant comprises at least 5, at least 15,preferably at least 25, more preferably at least 35, or even morepreferably at least 40 or more of the following amino acidsubstitutions: S24C, L26R, L26G, R28D, R28Y, R30H, N32A, N32S, K34D,K34V, S35L, S36R, V37A, V37S, S40R, E42R, G44A, G44S, Q46E, T48V, T48S,V68T, V68K, A70Y, S72A, S78R, K80Q, D92G, V116L, L138M, T143N, S159P,F168L, E178D, C180S, F182V, F182M, N184E, I186K, I186M, S188R, S188N,K189R, S190N, K191P, K191N, L192V, G193K, G193I, Q195G, Q195R, Q197R,V199R, S201G, T203S, K207R, Y223R, K225V, K227N, F232H, D236E, and V238Iof any one of SEQ ID NOs: 1-5, or a biologically active fragmentthereof.

In further embodiments, the HE variant comprises at least 5, at least15, preferably at least 25, more preferably at least 35, or even morepreferably at least 40 or more of the following amino acidsubstitutions: S24C, L26R, R28D, N32A, K34D, S35L, S36R, V37A, S40R,E42R, G44A, Q46E, T48V, V68T, A70Y, S72A, S78R, K80Q, L138M, T143N,F168L, E178D, C180S, F182V, N184E, I186K, S188R, K189R, K191P, L192V,G193K, Q195G, Q197R, V199R, K207R, Y223R, K225V, K227N, F232H, D236E,and V238I of any one of SEQ ID NOs: 1-5, or a biologically activefragment thereof.

In particular embodiments, the HE variant comprises at least 5, at least15, preferably at least 25, more preferably at least 35, or even morepreferably at least 40 or more of the following amino acidsubstitutions: S24C, L26R, R28D, N32A, K34D, S35L, S36R, V37A, S40R,E42R, G44A, Q46E, T48V, V68T, A70Y, S72A, S78R, K80Q, L138M, T143N,S159P, F168L, E178D, C180S, F182M, N184E, I186M, S188N, S190N, K191N,L192V, G193I, Q195R, Q197R, V199R, T203S, K207R, Y223R, K225V, K227N,F232H, D236E, and V238I of any one of SEQ ID NOs: 1-5, or a biologicallyactive fragment thereof.

In certain embodiments, the HE variant comprises at least 5, at least15, preferably at least 25, more preferably at least 35, or even morepreferably at least 40 or more of the following amino acidsubstitutions: S24C, L26R, R28D, N32A, K34D, S35L, S36R, V37A, S40R,E42R, G44S, Q46E, T48S, V68T, A70Y, S72A, S78R, K80Q, D92G, V116L,L138M, T143N, S159P, F168L, E178D, C180S, F182M, N184E, I186M, S188N,S190N, K191N, L192V, G193I, Q195R, Q197R, V199R, T203S, K207R, Y223R,K225V, K227N, F232H, D236E, and V238I of any one of SEQ ID NOs: 1-5, ora biologically active fragment thereof.

In some embodiments, the HE variant comprises at least 5, at least 15,preferably at least 25, more preferably at least 35, or even morepreferably at least 40 or more of the following amino acidsubstitutions: S24C, L26R, R28D, R30H, N32A, K34V, S35L, S36R, V37S,S40R, E42R, G44S, Q46E, T48V, V68T, V68K, A70Y, S72A, S78R, K80Q, L138M,T143N, S159P, F168L, E178D, C180S, F182M, N184E, I186M, S188N, S190N,K191N, L192V, G193I, Q195R, Q197R, V199R, T203S, K207R, Y223R, K225V,K227N, F232H, D236E, and V238I of any one of SEQ ID NOs: 1-5, or abiologically active fragment thereof.

In particular embodiments, the HE variant comprises at least 5, at least15, preferably at least 25, more preferably at least 35, or even morepreferably at least 40 or more of the following amino acidsubstitutions: S24C, L26G, R28Y, R30H, N32S, K34V, S35L, S36R, V37S,S40R, E42R, G44S, Q46E, T48S, V68T, A70Y, S72A, S78R, K80Q, V116L,L138M, T143N, S159P, F168L, E178D, C180S, F182M, N184E, I186M, S188N,S190N, K191N, L192V, G193I, Q195R, Q197R, V199R, T203S, K207R, Y223R,K225V, K227N, F232H, D236E, and V238I of any one of SEQ ID NOs: 1-5, ora biologically active fragment thereof.

In certain embodiments, the HE variant comprises at least 5, at least15, preferably at least 25, more preferably at least 35, or even morepreferably at least 40 or more of the following amino acidsubstitutions: S24C, L26R, R28D, R30H, N32A, K34V, S35L, S36R, V37S,S40R, E42R, G44S, Q46E, T48V, V68T, A70Y, S72A, S78R, K80Q, V116L,L138M, T143N, S159P, F168L, E178D, C180S, F182V, N184E, I186K, S188R,K189R, K191P, L192V, G193K, Q195G, Q197R, V199R, S201G, K207R, Y223R,K225V, K227N, F232H, D236E, and V238I of any one of SEQ ID NOs: 1-5, ora biologically active fragment thereof.

In further embodiments, the HE variant comprises at least 5, at least15, preferably at least 25, more preferably at least 35, or even morepreferably at least 40 or more of the following amino acidsubstitutions: S24C, L26R, R28D, N32A, K34D, S35L, S36R, V37A, S40R,E42R, G44A, Q46E, T48V, V68T, A70Y, S72A, S78R, K80Q, D92G, L138M,T143N, S159P, F168L, E178D, C180S, F182M, N184E, I186M, S188N, S190N,K191N, L192V, G193I, Q195R, Q197R, V199R, T203S, K207R, Y223R, K225V,K227N, F232H, D236E, and V238I of any one of SEQ ID NOs: 1-5, or abiologically active fragment thereof.

In particular embodiments, the HE variant comprises an amino acidsequence that is at least 80%, preferably at least 85%, more preferablyat least 90%, or even more preferably at least 95% identical to theamino acid sequence set forth in any one of SEQ ID NOs: 6-12, or abiologically active fragment thereof.

In some embodiments, the HE variant comprises the amino acid sequenceset forth in SEQ ID NO: 6, or a biologically active fragment thereof.

In additional embodiments, the HE variant comprises the amino acidsequence set forth in SEQ ID NO: 7, or a biologically active fragmentthereof.

In particular embodiments, the HE variant comprises the amino acidsequence set forth in SEQ ID NO: 8, or a biologically active fragmentthereof.

In particular embodiments, the HE variant comprises the amino acidsequence set forth in SEQ ID NO: 9, or a biologically active fragmentthereof.

In further embodiments, the HE variant comprises the amino acid sequenceset forth in SEQ ID NO: 10, or a biologically active fragment thereof.

In certain embodiments, the HE variant comprises the amino acid sequenceset forth in SEQ ID NO: 11, or a biologically active fragment thereof.

In certain embodiments, the HE variant comprises the amino acid sequenceset forth in SEQ ID NO: 12, or a biologically active fragment thereof.

In some embodiments, the polypeptide binds the polynucleotide sequenceset forth in SEQ ID NO: 20.

In particular embodiments, the polypeptide further comprises a DNAbinding domain.

In additional embodiments, the DNA binding domain is selected from thegroup consisting of: a TALE DNA binding domain and a zinc finger DNAbinding domain.

In certain embodiments, the TALE DNA binding domain comprises about 9.5TALE repeat units to about 15.5 TALE repeat units.

In further embodiments, the TALE DNA binding domain binds apolynucleotide sequence in the CBLB gene.

In particular embodiments, the TALE DNA binding domain binds thepolynucleotide sequence set forth in SEQ ID NO: 21.

In particular embodiments, the polypeptide binds and cleaves thepolynucleotide sequence set forth in SEQ ID NO: 22.

In particular embodiments, the zinc finger DNA binding domain comprises2, 3, 4, 5, 6, 7, or 8 zinc finger motifs.

In additional embodiments, the polypeptide further comprises a peptidelinker and an end-processing enzyme or biologically active fragmentthereof.

In certain embodiments, the polypeptide further comprises a viralself-cleaving 2A peptide and an end-processing enzyme or biologicallyactive fragment thereof.

In further embodiments, the end-processing enzyme or biologically activefragment thereof has 5′-3′ exonuclease, 5′-3′ alkaline exonuclease,3′-5′ exonuclease, 5′ flap endonuclease, helicase, TdT, ortemplate-independent DNA polymerase activity.

In some embodiments, the end-processing enzyme comprises Trex2 or abiologically active fragment thereof.

In further embodiments, the polypeptide comprises the amino acidsequence set forth in any one of SEQ ID NOs: 13-19, or a biologicallyactive fragment thereof.

In additional embodiments, the polypeptide comprises the amino acidsequence set forth in SEQ ID NO: 13, or a biologically active fragmentthereof.

In particular embodiments, the polypeptide comprises the amino acidsequence set forth in SEQ ID NO: 14, or a biologically active fragmentthereof.

In certain embodiments, the polypeptide comprises the amino acidsequence set forth in SEQ ID NO: 15, or a biologically active fragmentthereof.

In certain embodiments, the polypeptide comprises the amino acidsequence set forth in SEQ ID NO: 16, or a biologically active fragmentthereof.

In some embodiments, the polypeptide comprises the amino acid sequenceset forth in SEQ ID NO: 17, or a biologically active fragment thereof.

In particular embodiments, the polypeptide comprises the amino acidsequence set forth in SEQ ID NO: 18, or a biologically active fragmentthereof.

In further embodiments, the polypeptide comprises the amino acidsequence set forth in SEQ ID NO: 19, or a biologically active fragmentthereof.

In particular embodiments, the polypeptide cleaves the human CBLB geneat a polynucleotide sequence set forth in SEQ ID NOs: 20 or 22.

In various embodiments, the present disclosure provides, in part, apolynucleotide encoding a polypeptide contemplated herein.

In some embodiments, the present disclosure provides, in part, an mRNAencoding a polypeptide contemplated herein.

In particular embodiments, the present disclosure provides, in part, acDNA encoding a polypeptide contemplated herein.

In various embodiments, the present disclosure provides, in part, avector comprising a polynucleotide encoding a polypeptide contemplatedherein.

In various embodiments, the present disclosure provides, in part, a cellcomprising a polypeptide contemplated herein.

In additional embodiments, the present disclosure provides, in part, acell comprising a polynucleotide encoding a polypeptide contemplatedherein.

In further embodiments, the present disclosure provides, in part, a cellcomprising a vector contemplated herein.

In some embodiments, the present disclosure provides, in part, a cellcomprising one or more genome modifications introduced by a polypeptidecontemplated herein.

In particular embodiments, the cell comprises a polynucleotide encodingone or more of an immunopotency enhancer, an immunosuppressive signaldamper, or an engineered antigen receptor.

In further embodiments, the polynucleotide further comprises an RNApolymerase II promoter operably linked to the polynucleotide encodingthe immunopotency enhancer, immunosuppressive signal damper, orengineered antigen receptor.

In some embodiments, the RNA polymerase II promoter is selected from thegroup consisting of: a short EF1α promoter, a long EF1α promoter, ahuman ROSA 26 locus, a Ubiquitin C (UBC) promoter, a phosphoglyceratekinase-1 (PGK) promoter, a cytomegalovirus enhancer/chicken β-actin(CAG) promoter, a β-actin promoter and a myeloproliferative sarcomavirus enhancer, negative control region deleted, dl587rev primer-bindingsite substituted (MND) promoter.

In additional embodiments, the polynucleotide further encodes one ormore self-cleaving viral peptides operably linked to, interspersedbetween, and/or flanking the immunopotency enhancer, immunosuppressivesignal damper, or engineered antigen receptor.

In particular embodiments, the self-cleaving viral peptide is a 2Apeptide.

In certain embodiments, the polynucleotide further comprises aheterologous polyadenylation signal.

In particular embodiments, the immunosuppressive signal damper comprisesan enzymatic function that counteracts an immunosuppressive factor.

In additional embodiments, the immunosuppressive signal damper compriseskynureninase activity.

In particular embodiments, the immunosuppressive signal dampercomprises: an exodomain that binds an immunosuppressive factor,optionally wherein the exodomain is an antibody or antigen bindingfragment thereof; an exodomain that binds an immunosuppressive factorand a transmembrane domain; or an exodomain that binds animmunosuppressive factor, a transmembrane domain, and a modifiedendodomain that is unable to transduce immunosuppressive signals to thecell.

In further embodiments, the immunopotency enhancer is selected from thegroup consisting of: a bispecific T cell engager molecule (BiTE), animmunopotentiating factor, and a flip receptor.

In some embodiments, the immunopotentiating factor is selected from thegroup consisting of: a cytokine, a chemokine, a cytotoxin, a cytokinereceptor, and variants thereof.

In some embodiments, the flip receptor comprises a TGFβRII exodomain andtransmembrane domain; and an endodomain from TLR4, CD28, CD134, CD137,CD278, and/or CD3ζ fused in frame to the C-terminal end of the TGFβRIItransmembrane domain.

In particular embodiments, the flip receptor comprises a TGFβRIIexodomain; a transmembrane domain isolated from a TLR4, CD3, CD4, CD8α,CD28, CD134, or CD137 polypeptide; and an endodomain from TLR4, CD28,CD134, CD137, CD278, and/or CD3ζ fused in frame to the C-terminal end ofthe TGFβRII exodomain.

In certain embodiments, the flip receptor comprises a TGFβRII exodomain;and a transmembrane domain and endodomain isolated from a TLR4, CD3,CD4, CD8α, CD28, CD134, or CD137 polypeptide fused in frame to theC-terminal end of the TGFβRII exodomain.

In particular embodiments, the engineered antigen receptor is selectedfrom the group consisting of: an engineered TCR, a CAR, a Daric, or azetakine.

In additional embodiments, the engineered receptor is not integratedinto the CBLB gene.

In further embodiments, the polynucleotide encoding one or more of animmunopotency enhancer, an immunosuppressive signal damper, or anengineered antigen receptor is integrated into the CBLB gene.

In further embodiments, a donor repair template comprises thepolynucleotide encoding one or more of an immunopotency enhancer, animmunosuppressive signal damper, or an engineered antigen receptor isintegrated into the CBLB gene at a DNA double stranded break siteintroduced by a polypeptide contemplated herein.

In particular embodiments, the cell is a hematopoietic cell.

In some embodiments, the cell is a T cell.

In particular embodiments, the cell is a CD3+, CD4+, and/or CD8+ cell.

In additional embodiments, the cell is an immune effector cell.

In particular embodiments, the cell is a cytotoxic T lymphocytes (CTLs),a tumor infiltrating lymphocytes (TILs), or a helper T cells.

In certain embodiments, the cell is a natural killer (NK) cell ornatural killer T (NKT) cell.

In a preferred embodiment, the cell is a T cell that has beengenetically modified to express an engineered antigen receptor.

In a preferred embodiment, the cell is a T cell that has beengenetically modified to express a chimeric antigen receptor (CAR) orengineered T cell receptor (TCR).

In additional embodiments, the source of the cell is peripheral bloodmononuclear cells, bone marrow, lymph nodes tissue, cord blood, thymustissue, tissue from a site of infection, ascites, pleural effusion,spleen tissue, or tumors.

In some embodiments, the cell comprises one or more modified CBLBalleles.

In further embodiments, the one or more modified CBLB alleles arenon-functional or have substantially reduced CBLB function and/oractivity.

In particular embodiments, the cell comprises a nucleic acid encoding animmunopotency enhancer or immunosuppressive signal damper introducedinto the one or more modified CBLB alleles and the cell furthercomprises engineered antigen receptor that is not introduced into theone or more modifies CBLB alleles.

In some embodiments, the present disclosure provides, in part, aplurality of cells comprising one or more cells contemplated herein.

In various embodiments, the present disclosure provides, in part, acomposition comprising one or more cells contemplated herein.

In some embodiments, the present disclosure provides, in part, acomposition comprising one or more cells contemplated herein and aphysiologically acceptable carrier.

In particular embodiments, the present disclosure provides, in part, amethod of editing a human CBLB gene in a cell comprising: introducing apolynucleotide encoding a polypeptide contemplated herein into a cell,wherein expression of the polypeptide creates a double strand break at atarget site in a human CBLB gene.

In some embodiments, the present disclosure provides, in part, a methodof editing a human CBLB gene in cell comprising: introducing apolynucleotide encoding a polypeptide contemplated herein into the cell,wherein expression of the polypeptide creates a double strand break at atarget site in a human CBLB gene, wherein the break is repaired bynon-homologous end joining (NHEJ).

In certain embodiments, the present disclosure provides, in part, amethod of editing a human CBLB gene in a cell comprising: introducing apolynucleotide encoding a polypeptide contemplated herein and a donorrepair template into the cell, wherein expression of the polypeptidecreates a double strand break at a target site in a human CBLB gene andthe donor repair template is incorporated into the human CBLB gene byhomology directed repair (HDR) at the site of the double-strand break(DSB).

In particular embodiments, the cell is a hematopoietic cell.

In certain embodiments, the cell is a T cell.

In certain embodiments, the cell is a CD3+, CD4+, and/or CD8+ cell.

In some embodiments, the cell is an immune effector cell.

In additional embodiments, the cell is a cytotoxic T lymphocytes (CTLs),a tumor infiltrating lymphocytes (TILs), or a helper T cells.

In additional embodiments, the cell is a natural killer (NK) cell ornatural killer T (NKT) cell.

In particular embodiments, the source of the cell is peripheral bloodmononuclear cells, bone marrow, lymph nodes tissue, cord blood, thymustissue, tissue from a site of infection, ascites, pleural effusion,spleen tissue, or tumors.

In particular embodiments, the polynucleotide encoding the polypeptideis an mRNA.

In certain embodiments, a polynucleotide encoding a 5″-3″ exonuclease isintroduced into the cell.

In further embodiments, a polynucleotide encoding Trex2 or abiologically active fragment thereof is introduced into the cell.

In some embodiments, the donor repair template encodes a CBLB gene orportion thereof comprising one or more mutations compared to the wildtype CBLB gene.

In particular embodiments, the donor repair template encodes one or moreof an immunopotency enhancer, an immunosuppressive signal damper, or anengineered antigen receptor.

In some embodiments, the donor repair template further comprises an RNApolymerase II promoter operably linked to the immunopotency enhancer,immunosuppressive signal damper, or engineered antigen receptor.

In further embodiments, the RNA polymerase II promoter is selected fromthe group consisting of: a short EFla promoter, a long EFla promoter, ahuman ROSA 26 locus, a Ubiquitin C (UBC) promoter, a phosphoglyceratekinase-1 (PGK) promoter, a cytomegalovirus enhancer/chicken β-actin(CAG) promoter, a β-actin promoter and a myeloproliferative sarcomavirus enhancer, negative control region deleted, dl587rev primer-bindingsite substituted (MND) promoter.

In particular embodiments, the donor repair template further encodes oneor more self-cleaving viral peptides operably linked to, interspersedbetween, and/or flanking the immunopotency enhancer, immunosuppressivesignal damper, or engineered antigen receptor.

In additional embodiments, the self-cleaving viral peptide is a 2Apeptide.

In certain embodiments, the donor repair template further comprises aheterologous polyadenylation signal.

In further embodiments, the immunosuppressive signal damper comprises anenzymatic function that counteracts an immunosuppressive factor.

In particular embodiments, the immunosuppressive signal damper compriseskynureninase activity.

In some embodiments, the immunosuppressive signal damper comprises: anexodomain that binds an immunosuppressive factor, optionally wherein theexodomain is an antibody or antigen binding fragment thereof; anexodomain that binds an immunosuppressive factor and a transmembranedomain; or an exodomain that binds an immunosuppressive factor, atransmembrane domain, and a modified endodomain that is unable totransduce immunosuppressive signals to the cell.

In certain embodiments, the exodomain and/or transmembrane domain of theimmunosuppressive signal damper is the TGFβRII exodomain and/ortransmembrane domain.

In some embodiments, the immunopotency enhancer is selected from thegroup consisting of: a bispecific T cell engager molecule (BiTE), animmunopotentiating factor, and a flip receptor.

In particular embodiments, the immunopotentiating factor is selectedfrom the group consisting of: a cytokine, a chemokine, a cytotoxin, acytokine receptor, and variants thereof.

In additional embodiments, the flip receptor comprises a TGFβRIIexodomain and transmembrane domain; and an endodomain from TLR4, CD28,CD134, CD137, CD278, and/or CD3ζ fused in frame to the C-terminal end ofthe TGFβRII transmembrane domain.

In particular embodiments, the flip receptor comprises a TGFβRIIexodomain; a transmembrane domain isolated from a TLR4, CD3, CD4, CD8α,CD28, CD134, or CD137 polypeptide; and an endodomain from TLR4, CD28,CD134, CD137, CD278, and/or CD3ζ fused in frame to the C-terminal end ofthe TGFβRII exodomain.

In further embodiments, the flip receptor comprises a TGFβRII exodomain;and a transmembrane domain and endodomain isolated from a TLR4, CD3,CD4, CD8α, CD28, CD134, or CD137 polypeptide fused in frame to theC-terminal end of the TGFβRII exodomain.

In certain embodiments, the engineered antigen receptor is selected fromthe group consisting of: an engineered TCR, a CAR, a Daric, or azetakine.

In some embodiments, the donor repair template comprises a 5′ homologyarm homologous to a human CBLB gene sequence 5′ of the DSB and a 3′homology arm homologous to a human CBLB gene sequence 3′ of the DSB.

In further embodiments, the lengths of the 5′ and 3′ homology arms areindependently selected from about 100 bp to about 2500 bp.

In particular embodiments, the lengths of the 5′ and 3′ homology armsare independently selected from about 600 bp to about 1500 bp.

In particular embodiments, the 5′homology arm is about 1500 bp and the3′ homology arm is about 1000 bp.

In some embodiments, the 5′homology arm is about 600 bp and the 3′homology arm is about 600 bp.

In certain embodiments, a viral vector is used to introduce the donorrepair template into the cell.

In additional embodiments, the viral vector is a recombinantadeno-associated viral vector (rAAV) or a retrovirus.

In particular embodiments, the rAAV has one or more ITRs from AAV2.

In additional embodiments, the rAAV has a serotype selected from thegroup consisting of: AAV1, AAV2, AAV3, AAV4, AAV5, AAV6, AAV7, AAV8,AAV9, and AAV10.

In further embodiments, the rAAV has an AAV2 or AAV6 serotype.

In certain embodiments, the retrovirus is a lentivirus.

In some embodiments, the lentivirus is an integrase deficient lentivirus(IDLV).

In various embodiments, the present disclosure provides, in part, amethod of treating, preventing, or ameliorating at least one symptom ofa cancer, infectious disease, autoimmune disease, inflammatory disease,and immunodeficiency, or condition associated therewith, comprisingadministering to the subject an effective amount of a compositioncontemplated herein.

In certain embodiments, the present disclosure provides, in part, amethod of treating a solid cancer comprising administering to thesubject an effective amount of a composition contemplated herein.

In particular embodiments, the solid cancer comprises liver cancer,pancreatic cancer, lung cancer, breast cancer, ovarian cancer, prostatecancer, testicular cancer, bladder cancer, brain cancer, sarcoma, headand neck cancer, bone cancer, thyroid cancer, kidney cancer, or skincancer.

In some embodiments, the present disclosure provides, in part, a methodof treating a hematological malignancy comprising administering to thesubject an effective amount of a composition contemplated herein.

In certain embodiments, the hematological malignancy is a leukemia,lymphoma, or multiple myeloma.

BRIEF DESCRIPTION OF SEVERAL VIEWS OF THE DRAWINGS

FIG. 1 shows the CBLB gene and the HE target site in exon 6 (SEQ ID NOs:20 and 76), which encodes the SH2 domain.

FIG. 2 shows how the CBLB HE was reprogrammed via engineering of the NTDand CTD against chimeric ‘half-sites’ through three rounds of sorting,followed by fusion of the reprogrammed domains and screening against thecomplete CBLB target site to isolate a fully reprogrammed HE.

FIG. 3 shows the activity of CBLB HE variants in a chromosomal reporterassay.

FIG. 4 shows a yeast surface affinity titration of the CBLB.E3 HEvariant.

FIG. 5 shows an alignment of CBLB HE variants (SEQ ID NOs: 77-83) to thewild-type I-OnuI protein (SEQ ID NO:1), highlighting non-identicalpositions.

FIG. 6 shows the binding site (SEQ ID NOs: 22 and 84) for the TAL RVDsfused to the CBLB.E3 HE variant to generate a CBLB.E3 megaTAL.

FIG. 7 shows consistent CBLB gene editing rates in CAR T cells using aCBLB megaTAL.

FIG. 8 shows decreased intracellular CBLB protein expression in T cellstreated with a CBLB megaTAL.

FIG. 9 shows that CBL-edited T cells produce more IFNγ and TNFα whenstimulated by an anti-CD3 antibody, or by a CAR specific antigen.

FIG. 10 shows a TIDE analysis of T cells edited by co-delivery of mRNAsencoding various CBLB megaTALs and TREX2. Editing rate at the targetlocus was 61-93%.

FIG. 11 shows a diagram of an HDR strategy to insert a MND-GFPexpression cassette into a CBLB target site using a CBLB megaTAL and anAAV donor.

FIG. 12 shows a stable increase in GFP expression in T cells editedusing the HDR strategy depicted in FIG. 11 compared to mock edited Tcells.

FIG. 13 shows results of an in vivo mouse study. Mice with A549 tumorswere treated with vehicle treated T cells (upper left panel), T cellsedited with a CBLB megaTAL (upper right panel), anti-EGFR CAR T cells(lower left panel), and anti-EGFR CAR T cells edited with a CBLB megaTAL(lower right panel). Mean tumor volume was measured over time.

BRIEF DESCRIPTION OF THE SEQUENCE IDENTIFIERS

SEQ ID NO: 1 is an amino acid sequence of a wild type I-OnuI LAGLIDADGhoming endonuclease (LHE).

SEQ ID NO: 2 is an amino acid sequence of a wild type I-OnuI LHE.

SEQ ID NO: 3 is an amino acid sequence of a biologically active fragmentof a wild-type I-OnuI LHE.

SEQ ID NO: 4 is an amino acid sequence of a biologically active fragmentof a wild-type I-OnuI LHE.

SEQ ID NO: 5 is an amino acid sequence of a biologically active fragmentof a wild-type I-OnuI LHE.

SEQ ID NOs: 6-12 set forth amino acid sequences of I-OnuI LHE variantsreprogrammed to bind and cleave a target site in the human CBLB gene.

SEQ ID NOs: 13-19 set forth amino acid sequences of I-OnuI LHE variantsreprogrammed to bind and cleave a target site in the human CBLB gene.

SEQ ID NO: 20 is an I-OnuI LHE variant target site in exon 6 of a humanCBLB gene.

SEQ ID NO: 21 is a TALE DNA binding domain target site in exon 6 of ahuman CBLB gene.

SEQ ID NO: 22 is a megaTAL target site in exon 6 of a human CBLB gene.

SEQ ID NOs: 23, 25, 27, and 29 set forth I-OnuI LHE variant N-terminaldomain target sites in exon 6 of a human CBLB gene.

SEQ ID NOs: 24, 26, and 28 set forth I-OnuI LHE variant C-terminaldomain target sites in exon 6 of a human CBLB gene.

SEQ ID NO: 30 is a polynucleotide sequence of a CBLB.E3 surface displayplasmid.

SEQ ID NOs: 31-36 set forth-mRNA sequences encoding CBLB megaTALs.

SEQ ID NO: 37 is an mRNA sequence encoding murine Trex2.

SEQ ID NO: 38 is an amino acid sequence encoding murine Trex2.

SEQ ID NOs: 39-49 set forth the amino acid sequences of various linkers.

SEQ ID NOs: 50-74 set forth the amino acid sequences of proteasecleavage sites and self-cleaving polypeptide cleavage sites. In theforegoing sequences, X, if present, refers to any amino acid or theabsence of an amino acid.

DETAILED DESCRIPTION A. Overview

The present disclosure generally relates to, in part, improved genomeediting compositions and methods of use thereof. Without wishing to bebound by any particular theory, genome editing compositions contemplatedin various embodiments can be used to prevent or treat a cancer,infectious disease, autoimmune disease, inflammatory disease, andimmunodeficiency, or condition associated therewith, or ameliorate atleast one symptom thereof. One limitation or problem that vexes existingadoptive cell therapy is hyporesponsiveness of immune effector cells dueto exhaustion mediated by the tumor microenvironment. Exhausted T cellshave a unique molecular signature that is markedly distinct from naive,effector or memory T cells. Exhausted T cells are T cells with decreasedcytokine expression and effector function.

Casitas B-lineage (Cbl) lymphoma proto-oncogene B (CBLB) is a member ofthe RING-finger family or E3 ubiquitin ligases and is expressed in awide array of tissues and cell types including cells of thehematopoietic lineage. CBLB facilitates the ubiquitination of targetsubstrate proteins via the recruitment of E2-ubiquitin conjugatingenzymes to its RING finger domain. Ubiquitination of CBLB substrateproteins may promote protein degradation or interfere withprotein-protein interactions. CBLB binds to substrate proteins throughits SH2-containing tyrosine kinase binding domain, its proline-richsequences which interacts with SH3 domain-containing proteins, or itsubiquitin-associated domain which interacts with ubiquitin-taggedproteins.

CBLB is also involved in the negative regulation of effector T cellactivity and persistence. CBLB knockout mouse T cells arehyperproliferative, produce heightened levels of IL2 and IFNγ inresponse to antigen stimulation, are resistant to TGFβ-mediatedsuppression, and have a lower activation threshold indicating that CBLBplays a role in negatively regulating T cell activation. Without wishingto be bound by any particular theory, it is contemplated that disruptionof the CBLB gene in T cells using engineered nucleases will result inmore efficacious and persistent adoptive cellular immunotherapies.

In particular embodiments, genome edited immune effector cellscontemplated herein are made more resistant to exhaustion byeliminating, decreasing, or damping CBLB expression, CBLB activity,and/or signaling via CBLB.

Genome editing compositions and methods contemplated in variousembodiments comprise nuclease variants, designed to bind and cleave atarget site in the casitas B-lineage (Cbl) lymphoma proto-oncogene B(CBLB) gene. The nuclease variants contemplated in particularembodiments, can be used to introduce a double-strand break in a targetpolynucleotide sequence, which may be repaired by non-homologous endjoining (NHEJ) in the absence of a polynucleotide template, e.g., adonor repair template, or by homology directed repair (HDR), i.e.,homologous recombination, in the presence of a donor repair template.Nuclease variants contemplated in certain embodiments, can also bedesigned as nickases, which generate single-stranded DNA breaks that canbe repaired using the cell's base-excision-repair (BER) machinery orhomologous recombination in the presence of a donor repair template.NHEJ is an error-prone process that frequently results in the formationof small insertions and deletions that disrupt gene function. Homologousrecombination requires homologous DNA as a template for repair and canbe leveraged to create a limitless variety of modifications specified bythe introduction of donor DNA containing the desired sequence at thetarget site, flanked on either side by sequences bearing homology toregions flanking the target site.

In one preferred embodiment, the genome editing compositionscontemplated herein comprise a homing endonuclease variant or megaTALthat targets the human CBLB gene.

In one preferred embodiment, the genome editing compositionscontemplated herein comprise a homing endonuclease variant or megaTALand an end-processing enzyme, e.g., Trex2.

In various embodiments, genome edited cells are contemplated. The genomeedited cells comprise an edited CBLB gene, wherein the editing strategyis designed to decrease or eliminate CBLB expression. In particularembodiments, CAR T cells, engineered TCR T cells, or DARIC T cellcomprise an edited CBLB gene.

In various embodiments, a DNA break is generated in a target site of theCBLB gene in a T cell, e.g., immune effector cell, and NHEI of the endsof the cleaved genomic sequence may result in a cell with little or noCBLB expression, and preferably a T cell that lacks or substantiallylacks functional CBLB expression and/or signaling, e.g., lacks theability to increase T cell exhaustion. Without wishing to be bound byany particular theory, T cells that lack functional CBLB expression aremore resistant to immunosuppression and T cell exhaustion, and thus, aremore persistent and therapeutically efficacious.

In various other embodiments, a donor template for repair of the cleavedCBLB genomic sequence is provided. The CBLB gene is repaired with thesequence of the template by homologous recombination at the DNAbreak-site. In particular embodiments, the repair template comprises apolynucleotide sequence that disrupts, and preferably substantiallydecreases or eliminates, functional CBLB expression.

In particular embodiments, the CBLB gene is repaired with apolynucleotide encoding an immunopotency enhancer, immunosuppressivesignal damper, or engineered antigen receptor.

In particular embodiments, the CBLB gene is repaired with apolynucleotide encoding an immunopotency enhancer, immunosuppressivesignal damper, or engineered antigen receptor and is introduced into theCBLB gene so as to adopt the endogenous CBLB promoter totranscriptionally control the expression of the immunopotency enhancer,immunosuppressive signal damper, or engineered antigen receptor.

In preferred embodiments, the genome editing compositions and methodscontemplated herein are used to edit the human CBLB gene.

Accordingly, the methods and compositions contemplated herein representa quantum improvement compared to existing adoptive cell therapies.

Techniques for recombinant (i.e., engineered) DNA, peptide andoligonucleotide synthesis, immunoassays, tissue culture, transformation(e.g., electroporation, lipofection), enzymatic reactions, purificationand related techniques and procedures may be generally performed asdescribed in various general and more specific references inmicrobiology, molecular biology, biochemistry, molecular genetics, cellbiology, virology and immunology as cited and discussed throughout thepresent specification. See, e.g., Sambrook et al., Molecular Cloning: ALaboratory Manual, 3d ed., Cold Spring Harbor Laboratory Press, ColdSpring Harbor, N.Y.; Current Protocols in Molecular Biology (John Wileyand Sons, updated July 2008); Short Protocols in Molecular Biology: ACompendium of Methods from Current Protocols in Molecular Biology,Greene Pub. Associates and Wiley-Interscience; Glover, DNA Cloning: APractical Approach, vol. I & II (IRL Press, Oxford Univ. Press USA,1985); Current Protocols in Immunology (Edited by: John E. Coligan, AdaM. Kruisbeek, David H. Margulies, Ethan M. Shevach, Warren Strober 2001John Wiley & Sons, NY, N.Y.); Real-Time PCR: Current Technology andApplications, Edited by Julie Logan, Kirstin Edwards and Nick Saunders,2009, Caister Academic Press, Norfolk, UK; Anand, Techniques for theAnalysis of Complex Genomes, (Academic Press, New York, 1992); Guthrieand Fink, Guide to Yeast Genetics and Molecular Biology (Academic Press,New York, 1991); Oligonucleotide Synthesis (N. Gait, Ed., 1984); NucleicAcid The Hybridization (B. Hames & S. Higgins, Eds., 1985);Transcription and Translation (B. Hames & S. Higgins, Eds., 1984);Animal Cell Culture (R. Freshney, Ed., 1986); Perbal, A Practical Guideto Molecular Cloning (1984); Next-Generation Genome Sequencing (Janitz,2008 Wiley-VCH); PCR Protocols (Methods in Molecular Biology) (Park,Ed., 3rd Edition, 2010 Humana Press); Immobilized Cells And Enzymes (IRLPress, 1986); the treatise, Methods In Enzymology (Academic Press, Inc.,N.Y.); Gene Transfer Vectors For Mammalian Cells (J. H. Miller and M. P.Calos eds., 1987, Cold Spring Harbor Laboratory); Harlow and Lane,Antibodies, (Cold Spring Harbor Laboratory Press, Cold Spring Harbor,N.Y., 1998); Immunochemical Methods In Cell And Molecular Biology (Mayerand Walker, eds., Academic Press, London, 1987); Handbook OfExperimental Immunology, Volumes I-IV (D. M. Weir and C C Blackwell,eds., 1986); Roitt, Essential Immunology, 6th Edition, (BlackwellScientific Publications, Oxford, 1988); Current Protocols in Immunology(Q. E. Coligan, A. M. Kruisbeek, D. H. Margulies, E. M. Shevach and W.Strober, eds., 1991); Annual Review of Immunology; as well as monographsin journals such as Advances in Immunology.

B. Definitions

Prior to setting forth this disclosure in more detail, it may be helpfulto an understanding thereof to provide definitions of certain terms tobe used herein.

Unless defined otherwise, all technical and scientific terms used hereinhave the same meaning as commonly understood by those of ordinary skillin the art to which the invention belongs. Although any methods andmaterials similar or equivalent to those described herein can be used inthe practice or testing of particular embodiments, preferred embodimentsof compositions, methods and materials are described herein. For thepurposes of the present disclosure, the following terms are definedbelow. Additional definitions are set forth throughout this disclosure.

The articles “a,” “an,” and “the” are used herein to refer to one or tomore than one (i.e., to at least one, or to one or more) of thegrammatical object of the article. By way of example, “an element” meansone element or one or more elements.

The use of the alternative (e.g., “or”) should be understood to meaneither one, both, or any combination thereof of the alternatives.

The term “and/or” should be understood to mean either one, or both ofthe alternatives.

As used herein, the term “about” or “approximately” refers to aquantity, level, value, number, frequency, percentage, dimension, size,amount, weight or length that varies by as much as 15%, 10%, 9%, 8%, 7%,6%, 5%, 4%, 3%, 2% or 1% to a reference quantity, level, value, number,frequency, percentage, dimension, size, amount, weight or length. In oneembodiment, the term “about” or “approximately” refers a range ofquantity, level, value, number, frequency, percentage, dimension, size,amount, weight or length ±15%, ±10%, ±9%, ±8%, ±7%, ±6%, ±5%, ±4%, ±3%,±2%, or ±1% about a reference quantity, level, value, number, frequency,percentage, dimension, size, amount, weight or length.

In one embodiment, a range, e.g., 1 to 5, about 1 to 5, or about 1 toabout 5, refers to each numerical value encompassed by the range. Forexample, in one non-limiting and merely illustrative embodiment, therange “1 to 5” is equivalent to the expression 1, 2, 3, 4, 5; or 1.0,1.5, 2.0, 2.5, 3.0, 3.5, 4.0, 4.5, or 5.0; or 1.0, 1.1, 1.2, 1.3, 1.4,1.5, 1.6, 1.7, 1.8, 1.9, 2.0, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8,2.9, 3.0, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4.0, 4.1, 4.2,4.3, 4.4, 4.5, 4.6, 4.7, 4.8, 4.9, or 5.0.

As used herein, the term “substantially” refers to a quantity, level,value, number, frequency, percentage, dimension, size, amount, weight orlength that is 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%,99% or higher compared to a reference quantity, level, value, number,frequency, percentage, dimension, size, amount, weight or length. In oneembodiment, “substantially the same” refers to a quantity, level, value,number, frequency, percentage, dimension, size, amount, weight or lengththat produces an effect, e.g., a physiological effect, that isapproximately the same as a reference quantity, level, value, number,frequency, percentage, dimension, size, amount, weight or length.

Throughout this specification, unless the context requires otherwise,the words “comprise”, “comprises” and “comprising” will be understood toimply the inclusion of a stated step or element or group of steps orelements but not the exclusion of any other step or element or group ofsteps or elements. By “consisting of” is meant including, and limitedto, whatever follows the phrase “consisting of” Thus, the phrase“consisting of” indicates that the listed elements are required ormandatory, and that no other elements may be present. By “consistingessentially of” is meant including any elements listed after the phrase,and limited to other elements that do not interfere with or contributeto the activity or action specified in the disclosure for the listedelements. Thus, the phrase “consisting essentially of” indicates thatthe listed elements are required or mandatory, but that no otherelements are present that materially affect the activity or action ofthe listed elements.

Reference throughout this specification to “one embodiment,” “anembodiment,” “a particular embodiment,” “a related embodiment,” “acertain embodiment,” “an additional embodiment,” or “a furtherembodiment” or combinations thereof means that a particular feature,structure or characteristic described in connection with the embodimentis included in at least one embodiment. Thus, the appearances of theforegoing phrases in various places throughout this specification arenot necessarily all referring to the same embodiment. Furthermore, theparticular features, structures, or characteristics may be combined inany suitable manner in one or more embodiments. It is also understoodthat the positive recitation of a feature in one embodiment, serves as abasis for excluding the feature in a particular embodiment.

The term “ex vivo” refers generally to activities that take placeoutside an organism, such as experimentation or measurements done in oron living tissue in an artificial environment outside the organism,preferably with minimum alteration of the natural conditions. Inparticular embodiments, “ex vivo” procedures involve living cells ortissues taken from an organism and cultured or modulated in a laboratoryapparatus, usually under sterile conditions, and typically for a fewhours or up to about 24 hours, but including up to 48 or 72 hours,depending on the circumstances. In certain embodiments, such tissues orcells can be collected and frozen, and later thawed for ex vivotreatment. Tissue culture experiments or procedures lasting longer thana few days using living cells or tissue are typically considered to be“in vitro,” though in certain embodiments, this term can be usedinterchangeably with ex vivo.

The term “in vivo” refers generally to activities that take place insidean organism. In one embodiment, cellular genomes are engineered, edited,or modified in vivo.

By “enhance” or “promote” or “increase” or “expand” or “potentiate”refers generally to the ability of a nuclease variant, genome editingcomposition, or genome edited cell contemplated herein to produce,elicit, or cause a greater response (i.e., physiological response)compared to the response caused by either vehicle or control. Ameasurable response may include an increase in catalytic activity,binding affinity, binding site specificity, binding site selectivity,persistence, cytolytic activity, and/or an increase in proinflammatorycytokines, among others apparent from the understanding in the art andthe description herein. An “increased” or “enhanced” amount is typicallya “statistically significant” amount, and may include an increase thatis 1.1, 1.2, 1.5, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 30 or more times(e.g., 500, 1000 times) (including all integers and decimal points inbetween and above 1, e.g., 1.5, 1.6, 1.7. 1.8, etc.) the responseproduced by vehicle or control.

By “decrease” or “lower” or “lessen” or “reduce” or “abate” or “ablate”or “inhibit” or “dampen” refers generally to the ability of a nucleasevariant, genome editing composition, or genome edited cell contemplatedherein to produce, elicit, or cause a lesser response (i.e.,physiological response) compared to the response caused by eithervehicle or control. A measurable response may include a decrease inoff-target binding affinity, off-target cleavage specificity, T cellexhaustion, and the like. A “decrease” or “reduced” amount is typicallya “statistically significant” amount, and may include an decrease thatis 1.1, 1.2, 1.5, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 30 or more times(e.g., 500, 1000 times) (including all integers and decimal points inbetween and above 1, e.g., 1.5, 1.6, 1.7. 1.8, etc.) the response(reference response) produced by vehicle, or control.

By “maintain,” or “preserve,” or “maintenance,” or “no change,” or “nosubstantial change,” or “no substantial decrease” refers generally tothe ability of a nuclease variant, genome editing composition, or genomeedited cell contemplated herein to produce, elicit, or cause asubstantially similar or comparable physiological response (i.e.,downstream effects) in as compared to the response caused by eithervehicle or control. A comparable response is one that is notsignificantly different or measurable different from the referenceresponse.

The terms “specific binding affinity” or “specifically binds” or“specifically bound” or “specific binding” or “specifically targets” asused herein, describe binding of one molecule to another, e.g., DNAbinding domain of a polypeptide binding to DNA, at greater bindingaffinity than background binding. A binding domain “specifically binds”to a target site if it binds to or associates with a target site with anaffinity or K_(a) (i.e., an equilibrium association constant of aparticular binding interaction with units of 1/M) of, for example,greater than or equal to about 10⁵ M⁻¹. In certain embodiments, abinding domain binds to a target site with a K_(a) greater than or equalto about 10⁶ M⁻¹, 10⁷ M⁻¹, 10⁸ M⁻¹, 10⁹ M⁻¹, 10¹⁰ M⁻¹, 10¹¹ M⁻¹, 10¹²M⁻¹, or 10¹³ M⁻¹. “High affinity” binding domains refers to thosebinding domains with a K_(a) of at least 10⁷ M⁻¹, at least 10⁸ M⁻¹ atleast 10⁹ M⁻¹, at least 10¹⁰ M⁻¹, at least 10¹¹ M⁻¹, at least 10¹² M⁻¹,at least 10¹³ M⁻¹, or greater.

Alternatively, affinity may be defined in particular embodiments as anequilibrium dissociation constant (K_(d)) of a particular bindinginteraction with units of M (e.g., 10⁻⁵ M to 10⁻¹³ M, or less).Affinities of nuclease variants comprising one or more DNA bindingdomains for DNA target sites contemplated in particular embodiments canbe readily determined using conventional techniques, e.g., yeast cellsurface display, or by binding association, or displacement assays usinglabeled ligands.

In one embodiment, the affinity of specific binding is about 2 timesgreater than background binding, about 5 times greater than backgroundbinding, about 10 times greater than background binding, about 20 timesgreater than background binding, about 50 times greater than backgroundbinding, about 100 times greater than background binding, or about 1000times greater than background binding or more.

The terms “selectively binds” or “selectively bound” or “selectivelybinding” or “selectively targets” and describe preferential binding ofone molecule to a target molecule (on-target binding) in the presence ofa plurality of off-target molecules. In particular embodiments, an HE ormegaTAL selectively binds an on-target DNA binding site about 5, 10, 15,20, 25, 50, 100, or 1000 times more frequently than the HE or megaTALbinds an off-target DNA target binding site.

“On-target” refers to a target site sequence.

“Off-target” refers to a sequence similar to but not identical to atarget site sequence.

A “target site” or “target sequence” is a chromosomal orextrachromosomal nucleic acid sequence that defines a portion of anucleic acid to which a binding molecule will bind and/or cleave,provided sufficient conditions for binding and/or cleavage exist. Whenreferring to a polynucleotide sequence or SEQ ID NO. that referencesonly one strand of a target site or target sequence, it would beunderstood that the target site or target sequence bound and/or cleavedby a nuclease variant is double-stranded and comprises the referencesequence and its complement. In a preferred embodiment, the target siteis a sequence in a human CBLB gene.

“Recombination” refers to a process of exchange of genetic informationbetween two polynucleotides, including but not limited to, donor captureby non-homologous end joining (NHEJ) and homologous recombination. Forthe purposes of this disclosure, “homologous recombination (RR)” refersto the specialized form of such exchange that takes place, for example,during repair of double-strand breaks in cells via homology-directedrepair (HDR) mechanisms. This process requires nucleotide sequencehomology, uses a “donor” molecule as a template to repair a “target”molecule (i.e., the one that experienced the double-strand break), andis variously known as “non-crossover gene conversion” or “short tractgene conversion,” because it leads to the transfer of geneticinformation from the donor to the target. Without wishing to be bound byany particular theory, such transfer can involve mismatch correction ofheteroduplex DNA that forms between the broken target and the donor,and/or “synthesis-dependent strand annealing,” in which the donor isused to resynthesize genetic information that will become part of thetarget, and/or related processes. Such specialized HR often results inan alteration of the sequence of the target molecule such that part orall of the sequence of the donor polynucleotide is incorporated into thetarget polynucleotide.

“NHEJ” or “non-homologous end joining” refers to the resolution of adouble-strand break in the absence of a donor repair template orhomologous sequence. NHEJ can result in insertions and deletions at thesite of the break. NHEJ is mediated by several sub-pathways, each ofwhich has distinct mutational consequences. The classical NHEJ pathway(cNHEJ) requires the KU/DNA-PKcs/Lig4/XRCC4 complex, ligates ends backtogether with minimal processing and often leads to precise repair ofthe break. Alternative NHEJ pathways (altNHEJ) also are active inresolving dsDNA breaks, but these pathways are considerably moremutagenic and often result in imprecise repair of the break marked byinsertions and deletions. While not wishing to be bound to anyparticular theory, it is contemplated that modification of dsDNA breaksby end-processing enzymes, such as, for example, exonucleases, e.g.,Trex2, may increase the likelihood of imprecise repair.

“Cleavage” refers to the breakage of the covalent backbone of a DNAmolecule. Cleavage can be initiated by a variety of methods including,but not limited to, enzymatic or chemical hydrolysis of a phosphodiesterbond. Both single-stranded cleavage and double-stranded cleavage arepossible. Double-stranded cleavage can occur as a result of two distinctsingle-stranded cleavage events. DNA cleavage can result in theproduction of either blunt ends or staggered ends. In certainembodiments, polypeptides and nuclease variants, e.g., homingendonuclease variants, megaTALs, etc. contemplated herein are used fortargeted double-stranded DNA cleavage. Endonuclease cleavage recognitionsites may be on either DNA strand.

An “exogenous” molecule is a molecule that is not normally present in acell, but that is introduced into a cell by one or more genetic,biochemical or other methods. Exemplary exogenous molecules include, butare not limited to small organic molecules, protein, nucleic acid,carbohydrate, lipid, glycoprotein, lipoprotein, polysaccharide, anymodified derivative of the above molecules, or any complex comprisingone or more of the above molecules. Methods for the introduction ofexogenous molecules into cells are known to those of skill in the artand include, but are not limited to, lipid-mediated transfer (i.e.,liposomes, including neutral and cationic lipids), electroporation,direct injection, cell fusion, particle bombardment, biopolymernanoparticle, calcium phosphate co-precipitation, DEAE-dextran-mediatedtransfer and viral vector-mediated transfer.

An “endogenous” molecule is one that is normally present in a particularcell at a particular developmental stage under particular environmentalconditions. Additional endogenous molecules can include proteins.

A “gene,” refers to a DNA region encoding a gene product, as well as allDNA regions which regulate the production of the gene product, whetheror not such regulatory sequences are adjacent to coding and/ortranscribed sequences. A gene includes, but is not limited to, promotersequences, enhancers, silencers, insulators, boundary elements,terminators, polyadenylation sequences, post-transcription responseelements, translational regulatory sequences such as ribosome bindingsites and internal ribosome entry sites, replication origins, matrixattachment sites, and locus control regions.

“Gene expression” refers to the conversion of the information, containedin a gene, into a gene product. A gene product can be the directtranscriptional product of a gene (e.g., mRNA, tRNA, rRNA, antisenseRNA, ribozyme, structural RNA or any other type of RNA) or a proteinproduced by translation of an mRNA. Gene products also include RNAswhich are modified, by processes such as capping, polyadenylation,methylation, and editing, and proteins modified by, for example,methylation, acetylation, phosphorylation, ubiquitination,ADP-ribosylation, myristilation, and glycosylation.

As used herein, the term “genetically engineered” or “geneticallymodified” refers to the chromosomal or extrachromosomal addition ofextra genetic material in the form of DNA or RNA to the total geneticmaterial in a cell. Genetic modifications may be targeted ornon-targeted to a particular site in a cell's genome. In one embodiment,genetic modification is site specific. In one embodiment, geneticmodification is not site specific.

As used herein, the term “genome editing” refers to the substitution,deletion, and/or introduction of genetic material at a target site inthe cell's genome, which restores, corrects, disrupts, and/or modifiesexpression of a gene or gene product. Genome editing contemplated inparticular embodiments comprises introducing one or more nucleasevariants into a cell to generate DNA lesions at or proximal to a targetsite in the cell's genome, optionally in the presence of a donor repairtemplate.

As used herein, the term “gene therapy” refers to the introduction ofextra genetic material into the total genetic material in a cell thatrestores, corrects, or modifies expression of a gene or gene product, orfor the purpose of expressing a therapeutic polypeptide. In particularembodiments, introduction of genetic material into the cell's genome bygenome editing that restores, corrects, disrupts, or modifies expressionof a gene or gene product, or for the purpose of expressing atherapeutic polypeptide is considered gene therapy.

An “immune disorder” refers to a disease that evokes a response from theimmune system. In particular embodiments, the term “immune disorder”refers to a cancer, graft-versus-host disease, an autoimmune disease, oran immunodeficiency. In one embodiment, immune disorders encompassinfectious disease.

As used herein, the term “cancer” relates generally to a class ofdiseases or conditions in which abnormal cells divide without controland can invade nearby tissues.

As used herein, the term “malignant” refers to a cancer in which a groupof tumor cells display one or more of uncontrolled growth (i.e.,division beyond normal limits), invasion (i.e., intrusion on anddestruction of adjacent tissues), and metastasis (i.e., spread to otherlocations in the body via lymph or blood).

As used herein, the term “metastasize” refers to the spread of cancerfrom one part of the body to another. A tumor formed by cells that havespread is called a “metastatic tumor” or a “metastasis.” The metastatictumor contains cells that are like those in the original (primary)tumor.

As used herein, the term “benign” or “non-malignant” refers to tumorsthat may grow larger but do not spread to other parts of the body.Benign tumors are self-limited and typically do not invade ormetastasize.

A “cancer cell” or “tumor cell” refers to an individual cell of acancerous growth or tissue. A tumor refers generally to a swelling orlesion formed by an abnormal growth of cells, which may be benign,pre-malignant, or malignant. Most cancers form tumors, but some, e.g.,leukemia, do not necessarily form tumors. For those cancers that formtumors, the terms cancer (cell) and tumor (cell) are usedinterchangeably. The amount of a tumor in an individual is the “tumorburden” which can be measured as the number, volume, or weight of thetumor.

“Graft-versus-host disease” or “GVHD” refers complications that canoccur after cell, tissue, or solid organ transplant. GVHD can occurafter a stem cell or bone marrow transplant in which the transplanteddonor cells attack the transplant recipient's body. Acute GVHD in humanstakes place within about 60 days post-transplantation and results indamage to the skin, liver, and gut by the action of cytolyticlymphocytes. Chronic GVHD occurs later and is a systemic autoimmunedisease that affects primarily the skin, resulting in the polyclonalactivation of B cells and the hyperproduction of Ig and autoantibodies.Solid-organ transplant graft-versus-host disease (SOT-GVHD) occurs intwo forms. The more common type is antibody mediated, wherein antibodiesfrom a donor with blood type O attack a recipient's red blood cells inrecipients with blood type A, B, or AB, leading to mild transient,hemolytic anemias. The second form of SOT-GVHD is a cellular typeassociated with high mortality, wherein donor-derived T cells produce animmunological attack against immunologically disparate host tissue, mostoften in the skin, liver, gastrointestinal tract, and bone marrow,leading to complications in these organs.

“Graft-versus-leukemia” or “GVL” refer to an immune response to aperson's leukemia cells by immune cells present in a donor'stransplanted tissue, such as bone marrow or peripheral blood.

An “autoimmune disease” refers to a disease in which the body producesan immunogenic (i.e., immune system) response to some constituent of itsown tissue. In other words, the immune system loses its ability torecognize some tissue or system within the body as “self” and targetsand attacks it as if it were foreign. Illustrative examples ofautoimmune diseases include, but are not limited to: arthritis,inflammatory bowel disease, Hashimoto's thyroiditis, Grave's disease,lupus, multiple sclerosis, rheumatic arthritis, hemolytic anemia,anti-immune thyroiditis, systemic lupus erythematosus, celiac disease,Crohn's disease, colitis, diabetes, scleroderma, psoriasis, and thelike.

An “immunodeficiency” means the state of a patient whose immune systemhas been compromised by disease or by administration of chemicals. Thiscondition makes the system deficient in the number and type of bloodcells needed to defend against a foreign substance. Immunodeficiencyconditions or diseases are known in the art and include, for example,AIDS (acquired immunodeficiency syndrome), SCID (severe combinedimmunodeficiency disease), selective IgA deficiency, common variableimmunodeficiency, X-linked agammaglobulinemia, chronic granulomatousdisease, hyper-IgM syndrome, Wiskott-Aldrich Syndrome (WAS), anddiabetes.

An “infectious disease” refers to a disease that can be transmitted fromperson to person or from organism to organism, and is caused by amicrobial or viral agent (e.g., common cold). Infectious diseases areknown in the art and include, for example, hepatitis, sexuallytransmitted diseases (e.g., Chlamydia, gonorrhea), tuberculosis,HIV/AIDS, diphtheria, hepatitis B, hepatitis C, cholera, and influenza.

As used herein, the terms “individual” and “subject” are often usedinterchangeably and refer to any animal that exhibits a symptom of animmune disorder that can be treated with the nuclease variants, genomeediting compositions, gene therapy vectors, genome editing vectors,genome edited cells, and methods contemplated elsewhere herein. Suitablesubjects (e.g., patients) include laboratory animals (such as mouse,rat, rabbit, or guinea pig), farm animals, and domestic animals or pets(such as a cat or dog). Non-human primates and, preferably, humansubjects, are included. Typical subjects include human patients thathave, have been diagnosed with, or are at risk of having an immunedisorder.

As used herein, the term “patient” refers to a subject that has beendiagnosed with an immune disorder that can be treated with the nucleasevariants, genome editing compositions, gene therapy vectors, genomeediting vectors, genome edited cells, and methods contemplated elsewhereherein.

As used herein “treatment” or “treating,” includes any beneficial ordesirable effect on the symptoms or pathology of a disease orpathological condition, and may include even minimal reductions in oneor more measurable markers of the disease or condition being treated,e.g., cancer, GVHD, infectious disease, autoimmune disease, inflammatorydisease, and immunodeficiency. Treatment can optionally involve delayingof the progression of the disease or condition. “Treatment” does notnecessarily indicate complete eradication or cure of the disease orcondition, or associated symptoms thereof.

As used herein, “prevent,” and similar words such as “prevention,”“prevented,” “preventing” etc., indicate an approach for preventing,inhibiting, or reducing the likelihood of the occurrence or recurrenceof, a disease or condition, e.g., cancer, GVHD, infectious disease,autoimmune disease, inflammatory disease, and immunodeficiency. It alsorefers to delaying the onset or recurrence of a disease or condition ordelaying the occurrence or recurrence of the symptoms of a disease orcondition. As used herein, “prevention” and similar words also includesreducing the intensity, effect, symptoms and/or burden of a disease orcondition prior to onset or recurrence of the disease or condition.

As used herein, the phrase “ameliorating at least one symptom of” refersto decreasing one or more symptoms of the disease or condition for whichthe subject is being treated, e.g., cancer, GVHD, infectious disease,autoimmune disease, inflammatory disease, and immunodeficiency. Inparticular embodiments, the disease or condition being treated is acancer, wherein the one or more symptoms ameliorated include, but arenot limited to, weakness, fatigue, shortness of breath, easy bruisingand bleeding, frequent infections, enlarged lymph nodes, distended orpainful abdomen (due to enlarged abdominal organs), bone or joint pain,fractures, unplanned weight loss, poor appetite, night sweats,persistent mild fever, and decreased urination (due to impaired kidneyfunction).

As used herein, the term “amount” refers to “an amount effective” or “aneffective amount” of a nuclease variant, genome editing composition, orgenome edited cell sufficient to achieve a beneficial or desiredprophylactic or therapeutic result, including clinical results.

A “prophylactically effective amount” refers to an amount of a nucleasevariant, genome editing composition, or genome edited cell sufficient toachieve the desired prophylactic result. Typically but not necessarily,since a prophylactic dose is used in subjects prior to or at an earlierstage of disease, the prophylactically effective amount is less than thetherapeutically effective amount.

A “therapeutically effective amount” of a nuclease variant, genomeediting composition, or genome edited cell may vary according to factorssuch as the disease state, age, sex, and weight of the individual, andthe ability to elicit a desired response in the individual. Atherapeutically effective amount is also one in which any toxic ordetrimental effects are outweighed by the therapeutically beneficialeffects. The term “therapeutically effective amount” includes an amountthat is effective to “treat” a subject (e.g., a patient). When atherapeutic amount is indicated, the precise amount of the compositionscontemplated in particular embodiments, to be administered, can bedetermined by a physician in view of the specification and withconsideration of individual differences in age, weight, tumor size,extent of infection or metastasis, and condition of the patient(subject).

C. Nuclease Variants

Nuclease variants contemplated in particular embodiments herein aresuitable for genome editing a target site in the CBLB gene and compriseone or more DNA binding domains and one or more DNA cleavage domains(e.g., one or more endonuclease and/or exonuclease domains), andoptionally, one or more linkers contemplated herein. The terms“reprogrammed nuclease,” “engineered nuclease,” or “nuclease variant”are used interchangeably and refer to a nuclease comprising one or moreDNA binding domains and one or more DNA cleavage domains, wherein thenuclease has been designed and/or modified from a parental or naturallyoccurring nuclease, to bind and cleave a double-stranded DNA targetsequence in a CBLB gene.

In particular embodiments, a nuclease variant binds and cleaves a targetsequence in exon 6 of a CBLB gene, preferably at SEQ ID NO: 20 in exon 6of a CBLB gene, and more preferably at the sequence “ATTC” in SEQ ID NO:20 in exon 6 of a CBLB gene.

The nuclease variant may be designed and/or modified from a naturallyoccurring nuclease or from a previous nuclease variant. Nucleasevariants contemplated in particular embodiments may further comprise oneor more additional functional domains, e.g., an end-processing enzymaticdomain of an end-processing enzyme that exhibits 5′-3′ exonuclease,5′-3′ alkaline exonuclease, 3′-5′exonuclease (e.g., Trex2), 5′ flapendonuclease, helicase, template-dependent DNA polymerases ortemplate-independent DNA polymerase activity.

Illustrative examples of nuclease variants that bind and cleave a targetsequence in the CBLB gene include, but are not limited to homingendonuclease (meganuclease) variants and megaTALs.

1. Homing Endonuclease (Meganuclease) Variants

In various embodiments, a homing endonuclease or meganuclease isreprogrammed to introduce a double-strand break (DSB) in a target sitein a CBLB gene. In particular embodiments, a homing endonuclease variantintroduces a double strand break in exon 6 of a CBLB gene, preferably atSEQ ID NO: 20 in exon 6 of a CBLB gene, and more preferably at thesequence “ATTC” in SEQ ID NO: 20 in exon 6 of a CBLB gene.

“Homing endonuclease” and “meganuclease” are used interchangeably andrefer to naturally-occurring homing endonucleases that recognize 12-45base-pair cleavage sites and are commonly grouped into five familiesbased on sequence and structure motifs: LAGLIDADG, GIY-YIG, HNH, His-Cysbox, and PD-(D/E)XK.

A “reference homing endonuclease” or “reference meganuclease” refers toa wild type homing endonuclease or a homing endonuclease found innature. In one embodiment, a “reference homing endonuclease” refers to awild type homing endonuclease that has been modified to increase basalactivity.

An “engineered homing endonuclease,” “reprogrammed homing endonuclease,”“homing endonuclease variant,” “engineered meganuclease,” “reprogrammedmeganuclease,” or “meganuclease variant” refers to a homing endonucleasecomprising one or more DNA binding domains and one or more DNA cleavagedomains, wherein the homing endonuclease has been designed and/ormodified from a parental or naturally occurring homing endonuclease, tobind and cleave a DNA target sequence in a CBLB gene. The homingendonuclease variant may be designed and/or modified from a naturallyoccurring homing endonuclease or from another homing endonucleasevariant. Homing endonuclease variants contemplated in particularembodiments may further comprise one or more additional functionaldomains, e.g., an end-processing enzymatic domain of an end-processingenzyme that exhibits 5′-3′ exonuclease, 5′-3′ alkaline exonuclease,3′-5′ exonuclease (e.g., Trex2), 5′ flap endonuclease, helicase,template dependent DNA polymerase or template-independent DNA polymeraseactivity.

Homing endonuclease (HE) variants do not exist in nature and can beobtained by recombinant DNA technology or by random mutagenesis. HEvariants may be obtained by making one or more amino acid alterations,e.g., mutating, substituting, adding, or deleting one or more aminoacids, in a naturally occurring HE or HE variant. In particularembodiments, a HE variant comprises one or more amino acid alterationsto the DNA recognition interface.

HE variants contemplated in particular embodiments may further compriseone or more linkers and/or additional functional domains, e.g., anend-processing enzymatic domain of an end-processing enzyme thatexhibits 5′-3′ exonuclease, 5′-3′ alkaline exonuclease, 3′-5′exonuclease (e.g., Trex2), 5′ flap endonuclease, helicase,template-dependent DNA polymerase or template-independent DNA polymeraseactivity. In particular embodiments, HE variants are introduced into a Tcell with an end-processing enzyme that exhibits 5′-3′ exonuclease,5′-3′ alkaline exonuclease, 3′-5′ exonuclease (e.g., Trex2), 5′ flapendonuclease, helicase, template-dependent DNA polymerase ortemplate-independent DNA polymerase activity. The HE variant and 3′processing enzyme may be introduced separately, e.g., in differentvectors or separate mRNAs, or together, e.g., as a fusion protein, or ina polycistronic construct separated by a viral self-cleaving peptide oran IRES element.

A “DNA recognition interface” refers to the HE amino acid residues thatinteract with nucleic acid target bases as well as those residues thatare adjacent. For each HE, the DNA recognition interface comprises anextensive network of side chain-to-side chain and side chain-to-DNAcontacts, most of which is necessarily unique to recognize a particularnucleic acid target sequence. Thus, the amino acid sequence of the DNArecognition interface corresponding to a particular nucleic acidsequence varies significantly and is a feature of any natural or HEvariant. By way of non-limiting example, a HE variant contemplated inparticular embodiments may be derived by constructing libraries of HEvariants in which one or more amino acid residues localized in the DNArecognition interface of the natural HE (or a previously generated HEvariant) are varied. The libraries may be screened for target cleavageactivity against each predicted CBLB target site using cleavage assays(see e.g., Jarjour et al., 2009. Nuc. Acids Res. 37(20): 6871-6880).

LAGLIDADG homing endonucleases (LHE) are the most well studied family ofhoming endonucleases, are primarily encoded in archaea and in organellarDNA in green algae and fungi, and display the highest overall DNArecognition specificity. LHEs comprise one or two LAGLIDADG catalyticmotifs per protein chain and function as homodimers or single chainmonomers, respectively. Structural studies of LAGLIDADG proteinsidentified a highly conserved core structure (Stoddard 2005),characterized by an αββαββα fold, with the LAGLIDADG motif belonging tothe first helix of this fold. The highly efficient and specific cleavageof LHE' s represent a protein scaffold to derive novel, highly specificendonucleases. However, engineering LHEs to bind and cleave anon-natural or non-canonical target site requires selection of theappropriate LHE scaffold, examination of the target locus, selection ofputative target sites, and extensive alteration of the LHE to alter itsDNA contact points and cleavage specificity, at up to two-thirds of thebase-pair positions in a target site.

In one embodiment, LHEs from which reprogrammed LHEs or LHE variants maybe designed include, but are not limited to I-CreI and I-SceI.

Illustrative examples of LHEs from which reprogrammed LHEs or LHEvariants may be designed include, but are not limited to I-AabMI,I-AaeMI, I-Anil, I-ApaMI, I-CapIII, I-CapIV, I-CkaMI, I-CpaMI, I-CpaMII,I-CpaMIII, I-CpaMIV, I-CpaMV, I-CpaV, I-CraMI, I-EjeMI, I-GpeMI, I-Gpil,I-GzeMI, I-GzeMII, I-HjeMI, I-Ltrl, I-LtrWI, I-MpeMI, I-MveMI, I-NcrII,I-Ncrl, I-NcrMI, I-OheMI, I-OnuI, I-OsoMI, I-OsoMIV, I-PanMI, I-PanMII,I-PanMIII, I-PnoMI, I-ScuMI, I-SmaMI, I-SscMI, and I-Vdi1 41I.

In one embodiment, the reprogrammed LHE or LHE variant is selected fromthe group consisting of: an I-CpaMI variant, an I-HjeMI variant, anI-OnuI variant, an I-PanMI variant, and an I-SmaMI variant.

In one embodiment, the reprogrammed LHE or LHE variant is an I-OnuIvariant. See e.g., SEQ ID NOs: 6-12.

In one embodiment, reprogrammed I-OnuI LHEs or I-OnuI variants targetingthe CBLB gene were generated from a natural I-OnuI or biologicallyactive fragment thereof (SEQ ID NOs: 1-5). In a preferred embodiment,reprogrammed I-OnuI LHEs or I-OnuI variants targeting the human CBLBgene were generated from an existing I-OnuI variant. In one embodiment,reprogrammed I-OnuI LHEs were generated against a human CBLB gene targetsite set forth in SEQ ID NO: 20.

In a particular embodiment, the reprogrammed I-OnuI LHE or I-OnuIvariant that binds and cleaves a human CBLB gene comprises one or moreamino acid substitutions in the DNA recognition interface. In particularembodiments, the I-OnuI LHE that binds and cleaves a human CBLB genecomprises at least 70%, at least 71%, at least 72%, at least 73%, atleast 74%, at least 75%, at least 76%, at least 77%, at least 78%, atleast 79%, at least 80%, at least 81%, at least 82%, at least 83%, atleast 84%, at least 85%, at least 86%, at least 87%, at least 88%, atleast 89%, at least 90%, at least 91%, at least 92%, at least 93%, atleast 94%, at least 95%, at least 96%, at least 97%, at least 98%, or atleast 99% sequence identity with the DNA recognition interface of I-OnuI(Taekuchi et al. 2011. Proc Natl Acad Sci U.S.A. 2011 Aug. 9; 108(32):13077-13082) or an I-OnuI LHE variant as set forth in any one of SEQ IDNOs: 6-12, biologically active fragments thereof, and/or furthervariants thereof.

In one embodiment, the I-OnuI LHE that binds and cleaves a human CBLBgene comprises at least 70%, more preferably at least 80%, morepreferably at least 85%, more preferably at least 90%, more preferablyat least 95%, more preferably at least 97%, more preferably at least 99%sequence identity with the DNA recognition interface of I-OnuI (Taekuchiet al. 2011. Proc Natl Acad Sci U.S.A. 2011 Aug. 9; 108(32):13077-13082) or an I-OnuI LHE variant as set forth in any one of SEQ IDNOs: 6-12, biologically active fragments thereof, and/or furthervariants thereof.

In a particular embodiment, an I-OnuI LHE variant that binds and cleavesa human CBLB gene comprises one or more amino acid substitutions ormodifications in the DNA recognition interface of an I-OnuI as set forthin any one of SEQ ID NOs: 1-12, biologically active fragments thereof,and/or further variants thereof.

In a particular embodiment, an I-OnuI LHE variant that binds and cleavesa human CBLB gene comprises one or more amino acid substitutions ormodifications in the DNA recognition interface, particularly in thesubdomains situated from positions 24-50, 68 to 82, 180 to 203 and 223to 240 of I-OnuI (SEQ ID NOs: 1-5) or an I-OnuI variant as set forth inany one of SEQ ID NOs: 6-12, biologically active fragments thereof,and/or further variants thereof.

In particular embodiments, the HE variant comprises one or more aminoacid substitutions in the DNA recognition interface at amino acidpositions selected from the group consisting of: 24, 26, 28, 30, 32, 34,35, 36, 37, 38, 40, 42, 44, 46, 48, 68, 70, 72, 75, 76, 78, 80, 82, 180,182, 184, 186, 188, 189, 190, 191, 192, 193, 195, 197, 199, 201, 203,223, 225, 227, 229, 231, 232, 234, 236, 238, and 240 of I-OnuI (SEQ IDNOs: 1-5) or an I-OnuI variant as set forth in any one of SEQ ID NOs:6-12, biologically active fragments thereof, and/or further variantsthereof.

In particular embodiments, the HE variant comprises one or more aminoacid substitutions at amino acid positions selected from the groupconsisting of: 19, 24, 26, 28, 30, 32, 34, 35, 36, 37, 38, 40, 42, 44,46, 48, 59, 68, 70, 72, 75, 76 77, 78, 80, 82, 168, 180, 182, 184, 186,188, 189, 190, 191, 192, 193, 195, 197, 199, 201, 203, 223, 225, 227,229, 231, 232, 234, 236, 238, and 240 of I-OnuI (SEQ ID NOs: 1-5) or anI-OnuI variant as set forth in any one of SEQ ID NOs: 6-12, biologicallyactive fragments thereof, and/or further variants thereof.

In a particular embodiment, an I-OnuI LHE variant that binds and cleavesa human CBLB gene comprises 5, 10, 15, 20, 25, 30, 35, or 40 or moreamino acid substitutions or modifications in the DNA recognitioninterface, particularly in the subdomains situated from positions 24-50,68 to 82, 180 to 203 and 223 to 240 of I-OnuI (SEQ ID NOs: 1-5) or anI-OnuI variant as set forth in any one of SEQ ID NOs: 6-12, biologicallyactive fragments thereof, and/or further variants thereof.

In a particular embodiment, an I-OnuI LHE variant that binds and cleavesa human CBLB gene comprises 5, 10, 15, 20, 25, 30, 35, or 40 or moreamino acid substitutions or modifications at amino acid positionsselected from the group consisting of: 24, 26, 28, 30, 32, 34, 35, 36,37, 38, 40, 42, 44, 46, 48, 68, 70, 72, 75, 76, 78, 80, 82, 180, 182,184, 186, 188, 189, 190, 191, 192, 193, 195, 197, 199, 201, 203, 223,225, 227, 229, 231, 232, 234, 236, 238, and 240 of I-OnuI (SEQ ID NOs:1-5) or an I-OnuI variant as set forth in any one of SEQ ID NOs: 6-12,biologically active fragments thereof, and/or further variants thereof.

In a particular embodiment, an I-OnuI LHE variant that binds and cleavesa human CBLB gene comprises 5, 10, 15, 20, 25, 30, 35, or 40 or moreamino acid substitutions or modifications at amino acid positionsselected from the group consisting of: 19, 24, 26, 28, 30, 32, 34, 35,36, 37, 38, 40, 42, 44, 46, 48, 59, 68, 70, 72, 75, 76 77, 78, 80, 82,168, 180, 182, 184, 186, 188, 189, 190, 191, 192, 193, 195, 197, 199,201, 203, 223, 225, 227, 229, 231, 232, 234, 236, 238, and 240 of I-OnuI(SEQ ID NOs: 1-5) or an I-OnuI variant as set forth in any one of SEQ IDNOs: 6-12, biologically active fragments thereof, and/or furthervariants thereof.

In one embodiment, an I-OnuI LHE variant that binds and cleaves a humanCBLB gene comprises one or more amino acid substitutions ormodifications at additional positions situated anywhere within theentire I-OnuI sequence. The residues which may be substituted and/ormodified include but are not limited to amino acids that contact thenucleic acid target or that interact with the nucleic acid backbone orwith the nucleotide bases, directly or via a water molecule. In onenon-limiting example, an I-OnuI LHE variant contemplated herein thatbinds and cleaves a human CBLB gene comprises one or more substitutionsand/or modifications, preferably at least 5, preferably at least 10,preferably at least 15, preferably at least 20, more preferably at least25, more preferably at least 30, even more preferably at least 35, oreven more preferably at least 40 or more amino acid substitutions in atleast one position selected from the position group consisting ofpositions: 24, 26, 28, 30, 32, 34, 35, 36, 37, 38, 40, 42, 44, 46, 48,68, 70, 72, 78, 80, 92, 116, 138, 143, 159, 168, 178, 180, 182, 184,186, 188, 189, 190, 191, 192, 193, 195, 197, 199, 201, 203, 207, 223,225, 227, 232, 236, and 238 of I-OnuI (SEQ ID NOs: 1-5) or an I-OnuIvariant as set forth in any one of SEQ ID NOs: 6-12, biologically activefragments thereof, and/or further variants thereof.

In certain embodiments, the HE variant cleaves a CBLB exon 6 target siteand comprises at least 5, at least 15, preferably at least 25, morepreferably at least 35, or even more preferably at least 40 or more ofthe following amino acid substitutions: S24C, L26R, L26G, R28D, R28Y,R30H, N32A, N32S, K34D, K34V, S35L, S36R, V37A, V37S, S40R, E42R, G44A,G44S, Q46E, T48V, T48S, V68T, V68K, A70Y, S72A, S78R, K80Q, D92G, V116L,L138M, T143N, S159P, F168L, E178D, C180S, F182V, F182M, N184E, I186K,I186M, S188R, S188N, K189R, S190N, K191P, K191N, L192V, G193K, G193I,Q195G, Q195R, Q197R, V199R, S201G, T203S, K207R, Y223R, K225V, K227N,F232H, D236E, and V238I of I-OnuI (SEQ ID NOs: 1-5) or an I-OnuI variantas set forth in any one of SEQ ID NOs: 6-12, biologically activefragments thereof, and/or further variants thereof.

In some embodiments, the HE variant cleaves a CBLB target site andcomprises at least 5, at least 15, preferably at least 25, morepreferably at least 35, or even more preferably at least 40 or more ofthe following amino acid substitutions: S24C, L26R, R28D, N32A, K34D,S35L, S36R, V37A, S40R, E42R, G44A, Q46E, T48V, V68T, A70Y, S72A, S78R,K80Q, L138M, T143N, F168L, E178D, C180S, F182V, N184E, I186K, S188R,K189R, K191P, L192V, G193K, Q195G, Q197R, V199R, K207R, Y223R, K225V,K227N, F232H, D236E, and V238I of I-OnuI (SEQ ID NOs: 1-5) or an I-OnuIvariant as set forth in any one of SEQ ID NOs: 6-12, biologically activefragments thereof, and/or further variants thereof.

In particular embodiments, the HE variant cleaves a CBLB target site andcomprises at least 5, at least 15, preferably at least 25, morepreferably at least 35, or even more preferably at least 40 or more ofthe following amino acid substitutions: S24C, L26R, R28D, N32A, K34D,S35L, S36R, V37A, S40R, E42R, G44A, Q46E, T48V, V68T, A70Y, S72A, S78R,K80Q, L138M, T143N, S159P, F168L, E178D, C180S, F182M, N184E, I186M,S188N, S190N, K191N, L192V, G193I, Q195R, Q197R, V199R, T203S, K207R,Y223R, K225V, K227N, F232H, D236E, and V238I of I-OnuI (SEQ ID NOs: 1-5)or an I-OnuI variant as set forth in any one of SEQ ID NOs: 6-12,biologically active fragments thereof, and/or further variants thereof.

In particular embodiments, the HE variant cleaves a CBLB target site andcomprises at least 5, at least 15, preferably at least 25, morepreferably at least 35, or even more preferably at least 40 or more ofthe following amino acid substitutions: S24C, L26R, R28D, N32A, K34D,S35L, S36R, V37A, S40R, E42R, G44S, Q46E, T48S, V68T, A70Y, S72A, S78R,K80Q, D92G, V116L, L138M, T143N, S159P, F168L, E178D, C180S, F182M,N184E, I186M, S188N, S190N, K191N, L192V, G193I, Q195R, Q197R, V199R,T203S, K207R, Y223R, K225V, K227N, F232H, D236E, and V238I of I-OnuI(SEQ ID NOs: 1-5) or an I-OnuI variant as set forth in any one of SEQ IDNOs: 6-12, biologically active fragments thereof, and/or furthervariants thereof.

In particular embodiments, the HE variant cleaves a CBLB target site andcomprises at least 5, at least 15, preferably at least 25, morepreferably at least 35, or even more preferably at least 40 or more ofthe following amino acid substitutions: S24C, L26R, R28D, R30H, N32A,K34V, S35L, S36R, V37S, S40R, E42R, G44S, Q46E, T48V, V68T, V68K, A70Y,S72A, S78R, K80Q, L138M, T143N, S159P, F168L, E178D, C180S, F182M,N184E, I186M, S188N, S190N, K191N, L192V, G193I, Q195R, Q197R, V199R,T203S, K207R, Y223R, K225V, K227N, F232H, D236E, and V238I of I-OnuI(SEQ ID NOs: 1-5) or an I-OnuI variant as set forth in any one of SEQ IDNOs: 6-12, biologically active fragments thereof, and/or furthervariants thereof.

In particular embodiments, the HE variant cleaves a CBLB target site andcomprises at least 5, at least 15, preferably at least 25, morepreferably at least 35, or even more preferably at least 40 or more ofthe following amino acid substitutions: S24C, L26G, R28Y, R30H, N32S,K34V, S35L, S36R, V37S, S40R, E42R, G44S, Q46E, T48S, V68T, A70Y, S72A,S78R, K80Q, V116L, L138M, T143N, S159P, F168L, E178D, C180S, F182M,N184E, I186M, S188N, S190N, K191N, L192V, G193I, Q195R, Q197R, V199R,T203S, K207R, Y223R, K225V, K227N, F232H, D236E, and V238I of I-OnuI(SEQ ID NOs: 1-5) or an I-OnuI variant as set forth in any one of SEQ IDNOs: 6-12, biologically active fragments thereof, and/or furthervariants thereof.

In particular embodiments, the HE variant cleaves a CBLB target site andcomprises at least 5, at least 15, preferably at least 25, morepreferably at least 35, or even more preferably at least 40 or more ofthe following amino acid substitutions: S24C, L26R, R28D, R30H, N32A,K34V, S35L, S36R, V37S, S40R, E42R, G44S, Q46E, T48V, V68T, A70Y, S72A,S78R, K80Q, V116L, L138M, T143N, S159P, F168L, E178D, C180S, F182V,N184E, I186K, S188R, K189R, K191P, L192V, G193K, Q195G, Q197R, V199R,S201G, K207R, Y223R, K225V, K227N, F232H, D236E, and V238I of I-OnuI(SEQ ID NOs: 1-5) or an I-OnuI variant as set forth in any one of SEQ IDNOs: 6-12, biologically active fragments thereof, and/or furthervariants thereof.

In particular embodiments, the HE variant cleaves a CBLB target site andcomprises at least 5, at least 15, preferably at least 25, morepreferably at least 35, or even more preferably at least 40 or more ofthe following amino acid substitutions: S24C, L26R, R28D, N32A, K34D,S35L, S36R, V37A, S40R, E42R, G44A, Q46E, T48V, V68T, A70Y, S72A, S78R,K80Q, D92G, L138M, T143N, S159P, F168L, E178D, C180S, F182M, N184E,I186M, S188N, S190N, K191N, L192V, G193I, Q195R, Q197R, V199R, T203S,K207R, Y223R, K225V, K227N, F232H, D236E, and V238I of I-OnuI (SEQ IDNOs: 1-5) or an I-OnuI variant as set forth in any one of SEQ ID NOs:6-12, biologically active fragments thereof, and/or further variantsthereof.

In particular embodiments, an I-OnuI LHE variant that binds and cleavesa human CBLB gene comprises an amino acid sequence that is at least 80%,preferably at least 85%, more preferably at least 90%, or even morepreferably at least 95% identical to the amino acid sequence set forthin any one of SEQ ID NOs: 6-12, or a biologically active fragmentthereof.

In particular embodiments, an I-OnuI LHE variant comprises an amino acidsequence set forth in any one of SEQ ID NOs: 6-12, or a biologicallyactive fragment thereof.

In particular embodiments, an I-OnuI LHE variant comprises an amino acidsequence set forth in SEQ ID NO: 6, or a biologically active fragmentthereof.

In particular embodiments, an I-OnuI LHE variant comprises an amino acidsequence set forth in SEQ ID NO: 7, or a biologically active fragmentthereof.

In particular embodiments, an I-OnuI LHE variant comprises an amino acidsequence set forth in SEQ ID NO: 8, or a biologically active fragmentthereof.

In particular embodiments, an I-OnuI LHE variant comprises an amino acidsequence set forth in SEQ ID NO: 9, or a biologically active fragmentthereof.

In particular embodiments, an I-OnuI LHE variant comprises an amino acidsequence set forth in SEQ ID NO: 10, or a biologically active fragmentthereof.

In particular embodiments, an I-OnuI LHE variant comprises an amino acidsequence set forth in SEQ ID NO: 11, or a biologically active fragmentthereof.

In particular embodiments, an I-OnuI LHE variant comprises an amino acidsequence set forth in SEQ ID NO: 12, or a biologically active fragmentthereof.

2. MegaTALs

In various embodiments, a megaTAL comprising a homing endonucleasevariant is reprogrammed to introduce a double-strand break (DSB) in atarget site in a CBLB gene. In particular embodiments, a megaTALintroduces a DSB in exon 6 of a CBLB gene, preferably at SEQ ID NO: 20in exon 6 of a CBLB gene, and more preferably at the sequence “ATTC” inSEQ ID NO: 20 in exon 6 of a CBLB gene.

A “megaTAL” refers to a polypeptide comprising a TALE DNA binding domainand a homing endonuclease variant that binds and cleaves a DNA targetsequence in a CBLB gene, and optionally comprises one or more linkersand/or additional functional domains, e.g., an end-processing enzymaticdomain of an end-processing enzyme that exhibits 5′-3′ exonuclease,5′-3′ alkaline exonuclease, 3′-5′ exonuclease (e.g., Trex2), 5′ flapendonuclease, helicase or template-independent DNA polymerase activity.

In particular embodiments, a megaTAL can be introduced into a cell alongwith an end-processing enzyme that exhibits 5′-3′ exonuclease, 5′-3′alkaline exonuclease, 3′-5′ exonuclease (e.g., Trex2), 5′ flapendonuclease, helicase, template-dependent DNA polymerase, ortemplate-independent DNA polymerase activity. The megaTAL and 3′processing enzyme may be introduced separately, e.g., in differentvectors or separate mRNAs, or together, e.g., as a fusion protein, or ina polycistronic construct separated by a viral self-cleaving peptide oran IRES element.

A “TALE DNA binding domain” is the DNA binding portion of transcriptionactivator-like effectors (TALE or TAL-effectors), which mimics planttranscriptional activators to manipulate the plant transcriptome (seee.g., Kay et al., 2007. Science 318:648-651). TALE DNA binding domainscontemplated in particular embodiments are engineered de novo or fromnaturally occurring TALEs, e.g., AvrBs3 from Xanthomonas campestris pv.vesicatoria, Xanthomonas gardneri, Xanthomonas translucens, Xanthomonasaxonopodis, Xanthomonas perforans, Xanthomonas alfalfa, Xanthomonascitri, Xanthomonas euvesicatoria, and Xanthomonas oryzae and brg11 andhpx17 from Ralstonia solanacearum. Illustrative examples of TALEproteins for deriving and designing DNA binding domains are disclosed inU.S. Pat. No. 9,017,967, and references cited therein, all of which areincorporated herein by reference in their entireties.

In particular embodiments, a megaTAL comprises a TALE DNA binding domaincomprising one or more repeat units that are involved in binding of theTALE DNA binding domain to its corresponding target DNA sequence. Asingle “repeat unit” (also referred to as a “repeat”) is typically 33-35amino acids in length. Each TALE DNA binding domain repeat unit includes1 or 2 DNA-binding residues making up the Repeat Variable Di-Residue(RVD), typically at positions 12 and/or 13 of the repeat. The natural(canonical) code for DNA recognition of these TALE DNA binding domainshas been determined such that an HD sequence at positions 12 and 13leads to a binding to cytosine (C), NG binds to T, NI to A, NN binds toG or A, and NG binds to T. In certain embodiments, non-canonical(atypical) RVDs are contemplated.

Illustrative examples of non-canonical RVDs suitable for use inparticular megaTALs contemplated in particular embodiments include, butare not limited to HH, KH, NH, NK, NQ, RH, RN, SS, NN, SN, KN forrecognition of guanine (G); NI, KI, RI, HI, SI for recognition ofadenine (A); NG, HG, KG, RG for recognition of thymine (T); RD, SD, HD,ND, KD, YG for recognition of cytosine (C); NV, HN for recognition of Aor G; and H*, HA, KA, N*, NA, NC, NS, RA, S* for recognition of A or Tor G or C, wherein (*) means that the amino acid at position 13 isabsent. Additional illustrative examples of RVDs suitable for use inparticular megaTALs contemplated in particular embodiments furtherinclude those disclosed in U.S. Pat. No. 8,614,092, which isincorporated herein by reference in its entirety.

In particular embodiments, a megaTAL contemplated herein comprises aTALE DNA binding domain comprising 3 to 30 repeat units. In certainembodiments, a megaTAL comprises 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13,14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30TALE DNA binding domain repeat units. In a preferred embodiment, amegaTAL contemplated herein comprises a TALE DNA binding domaincomprising 5-15 repeat units, more preferably 7-15 repeat units, morepreferably 9-15 repeat units, and more preferably 9, 10, 11, 12, 13, 14,or 15 repeat units.

In particular embodiments, a megaTAL contemplated herein comprises aTALE DNA binding domain comprising 3 to 30 repeat units and anadditional single truncated TALE repeat unit comprising 20 amino acidslocated at the C-terminus of a set of TALE repeat units, i.e., anadditional C-terminal half-TALE DNA binding domain repeat unit (aminoacids −20 to −1 of the C-cap disclosed elsewhere herein, infra). Thus,in particular embodiments, a megaTAL contemplated herein comprises aTALE DNA binding domain comprising 3.5 to 30.5 repeat units. In certainembodiments, a megaTAL comprises 3.5, 4.5, 5.5, 6.5, 7.5, 8.5, 9.5,10.5, 11.5, 12.5, 13.5, 14.5, 15.5, 16.5, 17.5, 18.5, 19.5, 20.5, 21.5,22.5, 23.5, 24.5, 25.5, 26.5, 27.5, 28.5, 29.5, or 30.5 TALE DNA bindingdomain repeat units. In a preferred embodiment, a megaTAL contemplatedherein comprises a TALE DNA binding domain comprising 5.5-15.5 repeatunits, more preferably 7.5-15.5 repeat units, more preferably 9.5-15.5repeat units, and more preferably 9.5, 10.5, 11.5, 12.5, 13.5, 14.5, or15.5 repeat units.

In particular embodiments, a megaTAL comprises a TAL effectorarchitecture comprising an “N-terminal domain (NTD)” polypeptide, one ormore TALE repeat domains/units, a “C-terminal domain (CTD)” polypeptide,and a homing endonuclease variant. In some embodiments, the NTD, TALErepeats, and/or CTD domains are from the same species. In otherembodiments, one or more of the NTD, TALE repeats, and/or CTD domainsare from different species.

As used herein, the term “N-terminal domain (NTD)” polypeptide refers tothe sequence that flanks the N-terminal portion or fragment of anaturally occurring TALE DNA binding domain. The NTD sequence, ifpresent, may be of any length as long as the TALE DNA binding domainrepeat units retain the ability to bind DNA. In particular embodiments,the NTD polypeptide comprises at least 120 to at least 140 or more aminoacids N-terminal to the TALE DNA binding domain (0 is amino acid 1 ofthe most N-terminal repeat unit). In particular embodiments, the NTDpolypeptide comprises at least about 120, 121, 122, 123, 124, 125, 126,127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 138, 139, or atleast 140 amino acids N-terminal to the TALE DNA binding domain. In oneembodiment, a megaTAL contemplated herein comprises an NTD polypeptideof at least about amino acids +1 to +122 to at least about +1 to +137 ofa Xanthomonas TALE protein (0 is amino acid 1 of the most N-terminalrepeat unit). In particular embodiments, the NTD polypeptide comprisesat least about 122, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132,133, 134, 135, 136, or 137 amino acids N-terminal to the TALE DNAbinding domain of a Xanthomonas TALE protein. In one embodiment, amegaTAL contemplated herein comprises an NTD polypeptide of at leastamino acids +1 to +121 of a Ralstonia TALE protein (0 is amino acid 1 ofthe most N-terminal repeat unit). In particular embodiments, the NTDpolypeptide comprises at least about 121, 122, 123, 124, 125, 126, 127,128, 129, 130, 131, 132, 133, 134, 135, 136, or 137 amino acidsN-terminal to the TALE DNA binding domain of a Ralstonia TALE protein.

As used herein, the term “C-terminal domain (CTD)” polypeptide refers tothe sequence that flanks the C-terminal portion or fragment of anaturally occurring TALE DNA binding domain. The CTD sequence, ifpresent, may be of any length as long as the TALE DNA binding domainrepeat units retain the ability to bind DNA. In particular embodiments,the CTD polypeptide comprises at least 20 to at least 85 or more aminoacids C-terminal to the last full repeat of the TALE DNA binding domain(the first 20 amino acids are the half-repeat unit C-terminal to thelast C-terminal full repeat unit). In particular embodiments, the CTDpolypeptide comprises at least about 20, 21, 22, 23, 24, 25, 26, 27, 28,29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 443, 44, 45, 46,47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64,65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75 , 76, 77, 78, 79, 80, 81, 82,83, 84, or at least 85 amino acids C-terminal to the last full repeat ofthe TALE DNA binding domain. In one embodiment, a megaTAL contemplatedherein comprises a CTD polypeptide of at least about amino acids −20 to−1 of a Xanthomonas TALE protein (−20 is amino acid 1 of a half-repeatunit C-terminal to the last C-terminal full repeat unit). In particularembodiments, the CTD polypeptide comprises at least about 20, 19, 18,17, 16, 15, 14, 13, 12, 11, 10, 9, 8, 7, 6, 5, 4, 3, 2, or 1 amino acidsC-terminal to the last full repeat of the TALE DNA binding domain of aXanthomonas TALE protein. In one embodiment, a megaTAL contemplatedherein comprises a CTD polypeptide of at least about amino acids −20 to−1 of a Ralstonia TALE protein (−20 is amino acid 1 of a half-repeatunit C-terminal to the last C-terminal full repeat unit). In particularembodiments, the CTD polypeptide comprises at least about 20, 19, 18,17, 16, 15, 14, 13, 12, 11, 10, 9, 8, 7, 6, 5, 4, 3, 2, or 1 amino acidsC-terminal to the last full repeat of the TALE DNA binding domain of aRalstonia TALE protein.

In particular embodiments, a megaTAL contemplated herein, comprises afusion polypeptide comprising a TALE DNA binding domain engineered tobind a target sequence, a homing endonuclease reprogrammed to bind andcleave a target sequence, and optionally an NTD and/or CTD polypeptide,optionally joined to each other with one or more linker polypeptidescontemplated elsewhere herein. Without wishing to be bound by anyparticular theory, it is contemplated that a megaTAL comprising TALE DNAbinding domain, and optionally an NTD and/or CTD polypeptide is fused toa linker polypeptide which is further fused to a homing endonucleasevariant. Thus, the TALE DNA binding domain binds a DNA target sequencethat is within about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, or15 nucleotides away from the target sequence bound by the DNA bindingdomain of the homing endonuclease variant. In this way, the megaTALscontemplated herein, increase the specificity and efficiency of genomeediting.

In one embodiment, a megaTAL comprises a homing endonuclease variant anda TALE DNA binding domain that binds a nucleotide sequence that iswithin about 4, 5, or 6 nucleotides, preferably, 5 or 6 nucleotidesupstream of the binding site of the reprogrammed homing endonuclease.

In one embodiment, a megaTAL comprises a homing endonuclease variant anda TALE DNA binding domain that binds the nucleotide sequence set forthin SEQ ID NO: 21, which is 5 nucleotides upstream (i.e., there are 4nucleotides between the TALE binding site and the HE binding site) ofthe nucleotide sequence bound and cleaved by the homing endonucleasevariant (SEQ ID NO: 20). In preferred embodiments, the megaTAL targetsequence is SEQ ID NO: 22.

In particular embodiments, a megaTAL contemplated herein, comprises oneor more TALE DNA binding repeat units and an LHE variant designed orreprogrammed from an LHE selected from the group consisting of: I-AabMI,I-AaeMI, I-AniI, I-ApaMI, I-CapIII, I-CapIV, I-CkaMI, I-CpaMI, I-CpaMIV,I-CpaMV, I-CpaV, I-CraMI, I-EjeMI, I-GpeMI, I-GpiI, I-GzeMI, I-GzeMII,I-HjeMI, I-LtrI, I-LtrWI, I-MpeMI, I-MveMI, I-NcrII, I-Ncrl, I-NcrMI,I-OheMI, I-OnuI, I-OsoMI, I-OsoMIII, I-OsoMIV, I-PanMI, I-PanMII,I-PnoMI, I-ScuMI, I-SmaMI, I-SscMI, I-Vdi141I and variants thereof, orpreferably I-CpaMI, I-Hj eMI, I-OnuI, I-PanMI, SmaMI and variantsthereof, or more preferably I-OnuI and variants thereof.

In particular embodiments, a megaTAL contemplated herein, comprises anNTD, one or more TALE DNA binding repeat units, a CTD, and an LHEvariant selected from the group consisting of: I-AabMI, I-AaeMI, I-AniI,I-ApaMI, I-CapIII, I-CapIV, I-CkaMI, I-CpaMI, I-CpaMII, I-CpaMIII,I-CpaMIV, I-CpaMV, I-CpaV, I-CraMI, I-EjeMI, I-GpeMI, I-GpiI, I-GzeMI,I-GzeMIII, I-HjeMI, I-LtrII, I-LtrI, I-LtrWI, I-MpeMI, I-MveMI, I-Ncrl,I-NcrMI, I-OheMI, I-OnuI, I-OsoMI, I-OsoMIV, I-PanMI, I-PanMII, I-PnoMI,I-ScuMI, I-SmaMI, I-SscMI, I-Vdi141I and variants thereof, or preferablyI-CpaMI, I-HjeMI, I-OnuI, I-PanMI, SmaMI and variants thereof, or morepreferably I-OnuI and variants thereof.

In particular embodiments, a megaTAL contemplated herein, comprises anNTD, about 9.5 to about 15.5 TALE DNA binding repeat units, and an LHEvariant selected from the group consisting of: I-AabMI, I-AaeMI, I-Anil,I-ApaMI, I-CapIII, I-CapIV, I-CkaMI, I-CpaMI, I-CpaMIV, I-CpaMV, I-CpaV,I-CraMI, I-EjeMI, I-GpeMI, I-GpiI, I-GzeMI, I-HjeMI, I-LtrII, I-LtrI,I-LtrWI, I-MpeMI, I-MveMI, I-NcrII, I-Ncrl, I-NcrMI, I-OheMI, I-OnuI,I-OsoMI, I-OsoMII, I-OsoMIII, I-OsoMIV, I-PanMI, I-PanMII, I-PanMIII,I-PnoMI, I-ScuMI, I-SmaMI, I-SscMI, I-Vdi141I and variants thereof, orpreferably I-CpaMI, I-HjeMI, I-OnuI, I-PanMI, SmaMI and variantsthereof, or more preferably I-OnuI and variants thereof.

In particular embodiments, a megaTAL contemplated herein, comprises anNTD of about 122 amino acids to 137 amino acids, about 9.5, about 10.5,about 11.5, about 12.5, about 13.5, about 14.5, or about 15.5 bindingrepeat units, a CTD of about 20 amino acids to about 85 amino acids, andan I-OnuI LHE variant. In particular embodiments, any one of, two of, orall of the NTD, DNA binding domain, and CTD can be designed from thesame species or different species, in any suitable combination.

In particular embodiments, a megaTAL contemplated herein, comprises theamino acid sequence set forth in any one of SEQ ID NOs: 13-19.

In particular embodiments, a megaTAL-Trex2 fusion protein contemplatedherein, comprises the amino acid sequence set forth in any one of SEQ IDNOs: 13-19 and 38.

In certain embodiments, a megaTAL comprises a TALE DNA binding domainand an I-OnuI LHE variant binds and cleaves the nucleotide sequence setforth in SEQ ID NO: 22.

3. End-Processing Enzymes

Genome editing compositions and methods contemplated in particularembodiments comprise editing cellular genomes using a nuclease variantand one or more copies of an end-processing enzyme. In particularembodiments, a single polynucleotide encodes a homing endonucleasevariant and an end-processing enzyme, separated by a linker, aself-cleaving peptide sequence, e.g., 2A sequence, or by an IRESsequence. In particular embodiments, genome editing compositionscomprise a polynucleotide encoding a nuclease variant and a separatepolynucleotide encoding an end-processing enzyme. In particularembodiments, genome editing compositions comprise a polynucleotideencoding a homing endonuclease variant and an end-processing enzyme in asingle fusion polypeptide. In one embodiment, a fusion polypeptidecomprises a megaTAL and one or more copies of an end-processing enzyme,each separated by a self-cleaving peptide.

The term “end-processing enzyme” refers to an enzyme that modifies theexposed ends of a polynucleotide chain. The polynucleotide may bedouble-stranded DNA (dsDNA), single-stranded DNA (ssDNA), RNA,double-stranded hybrids of DNA and RNA, and synthetic DNA (for example,containing bases other than A, C, G, and T). An end-processing enzymemay modify exposed polynucleotide chain ends by adding one or morenucleotides, removing one or more nucleotides, removing or modifying aphosphate group and/or removing or modifying a hydroxyl group. Anend-processing enzyme may modify ends at endonuclease cut sites or atends generated by other chemical or mechanical means, such as shearing(for example by passing through fine-gauge needle, heating, sonicating,mini bead tumbling, and nebulizing), ionizing radiation, ultravioletradiation, oxygen radicals, chemical hydrolysis and chemotherapy agents.

In particular embodiments, genome editing compositions and methodscontemplated in particular embodiments comprise editing cellular genomesusing a homing endonuclease variant or megaTAL and a DNA end-processingenzyme.

The term “DNA end-processing enzyme” refers to an enzyme that modifiesthe exposed ends of DNA. A DNA end-processing enzyme may modify bluntends or staggered ends (ends with 5′ or 3′ overhangs). A DNAend-processing enzyme may modify single stranded or double stranded DNA.A DNA end-processing enzyme may modify ends at endonuclease cut sites orat ends generated by other chemical or mechanical means, such asshearing (for example by passing through fine-gauge needle, heating,sonicating, mini bead tumbling, and nebulizing), ionizing radiation,ultraviolet radiation, oxygen radicals, chemical hydrolysis andchemotherapy agents. DNA end-processing enzyme may modify exposed DNAends by adding one or more nucleotides, removing one or morenucleotides, removing or modifying a phosphate group and/or removing ormodifying a hydroxyl group.

Illustrative examples of DNA end-processing enzymes suitable for use inparticular embodiments contemplated herein include, but are not limitedto: 5′-3′ exonucleases, 5′-3′ alkaline exonucleases, 3′-5′ exonucleases,5′ flap endonucleases, helicases, phosphatases, hydrolases andtemplate-independent DNA polymerases.

Additional illustrative examples of DNA end-processing enzymes suitablefor use in particular embodiments contemplated herein include, but arenot limited to, Trex2, Trex1, Trex1 without transmembrane domain,Apollo, Artemis, DNA2, Exo1, ExoT, ExoIII, Fen1, Fan1, MreII, Rad2,Rad9, TdT (terminal deoxynucleotidyl transferase), PNKP, RecE, RecJ,RecQ, Lambda exonuclease, Sox, Vaccinia DNA polymerase, exonuclease I,exonuclease III, exonuclease VII, NDK1, NDK5, NDK7, NDK8, WRN,T7-exonuclease Gene 6, avian myeloblastosis virus integration protein(IN), Bloom, Antartic Phophatase, Alkaline Phosphatase, Poly nucleotideKinase (PNK), ApeI, Mung Bean nuclease, Hex1, TTRAP (TDP2), Sgs1, Sae2,CUP, Pol mu, Pol lambda, MUS81, EME1, EME2, SLX1, SLX4 and UL-12.

In particular embodiments, genome editing compositions and methods forediting cellular genomes contemplated herein comprise polypeptidescomprising a homing endonuclease variant or megaTAL and an exonuclease.The term “exonuclease” refers to enzymes that cleave phosphodiesterbonds at the end of a polynucleotide chain via a hydrolyzing reactionthat breaks phosphodiester bonds at either the 3′ or 5′ end.

Illustrative examples of exonucleases suitable for use in particularembodiments contemplated herein include, but are not limited to: hExoI,Yeast ExoI, E. coli ExoI, hTREX2, mouse TREX2, rat TREX2, hTREX1, mouseTREX1, and rat TREX1.

In particular embodiments, the DNA end-processing enzyme is a 3′ or 5′exonuclease, preferably Trex 1 or Trex2, more preferably Trex2, and evenmore preferably human or mouse Trex2.

D. Target Sites

Nuclease variants contemplated in particular embodiments can be designedto bind to any suitable target sequence and can have a novel bindingspecificity, compared to a naturally-occurring nuclease. In particularembodiments, the target site is a regulatory region of a gene including,but not limited to promoters, enhancers, repressor elements, and thelike. In particular embodiments, the target site is a coding region of agene or a splice site. In certain embodiments, nuclease variants aredesigned to down-regulate or decrease expression of a gene. Inparticular embodiments, a nuclease variant and donor repair template canbe designed to repair or delete a desired target sequence.

In various embodiments, nuclease variants bind to and cleave a targetsequence in a human casitas B-lineage (Cbl) lymphoma proto-oncogene B(CBLB) gene. CBL is also referred to as CBL2; Noonan syndrome-likedisorder with or without juvenile myelomonocytic leukemia (NSLL); C-CBL;RING finger protein 55 (RNF55); fragile site, folic acid type, rare, fra(11)(q23.3) (FRA11B); E3 ubiquitin-protein ligase CBL; Cas-Br-M (murine)ecotropic retroviral transforming sequence; Cbl proto-oncogene, E3ubiquitin protein ligase; RING-type E3 ubiquitin transferase CBL;casitas B-lineage lymphoma proto-oncogene; oncogene CBL2; proto-oncogenec-Cbl; and signal transduction protein CBL.

This gene is a proto-oncogene that encodes a RING finger E3 ubiquitinligase. The encoded protein is one of the enzymes required for targetingsubstrates for degradation by the proteasome. This protein mediates thetransfer of ubiquitin from ubiquitin conjugating enzymes (E2) tospecific substrates. This protein also contains an N-terminalphosphotyrosine binding domain that allows it to interact with numeroustyrosine-phosphorylated substrates and target them for proteasomedegradation. CBLB functions as a negative regulator of many signaltransduction pathways, including T cell activation and persistence.

In particular embodiments, a homing endonuclease variant or megaTALintroduces a double-strand break (DSB) in a target site in a CBLB gene.In particular embodiments, a homing endonuclease variant or megaTALintroduces a DSB in exon 6 of a CBLB gene, preferably at SEQ ID NO: 20in exon 6 of a CBLB gene, and more preferably at the sequence “ATTC” inSEQ ID NO: 20 in exon 6 of a CBLB gene.

In a preferred embodiment, a homing endonuclease variant or megaTALcleaves double-stranded DNA and introduces a DSB into the polynucleotidesequence set forth in SEQ ID NO: 20 or 22.

In a preferred embodiment, the CBLB gene is a human CBLB gene.

E. Donor Repair Templates

Nuclease variants may be used to introduce a DSB in a target sequence;the DSB may be repaired through homology directed repair (HDR)mechanisms in the presence of one or more donor repair templates.

In various embodiments, the donor repair template comprises one or morepolynucleotides encoding an immunopotency enhancer, an immunosuppressivesignal damper, or an engineered antigen receptor.

In various embodiments, it is contemplated that providing a cell anengineered nuclease in the presence of a plurality of donor repairtemplates independently encoding immunopotency enhancers and/orimmunosuppressive signal dampers targeting different immunosuppressivepathways, yields genome edited T cells with increased therapeuticefficacy and persistence. For example, immunopotency enhancers orimmunosuppressive signal targeting combinations of PD-1, LAG-3, CTLA-4,TIN/13, IL-10R, TIGIT, and TGFβRII pathways may be preferred inparticular embodiments.

In particular embodiments, the donor repair template is used to insert asequence into the genome. In particular preferred embodiments, the donorrepair template is used to repair or modify a sequence in the genome.

In various embodiments, a donor repair template is introduced into ahematopoietic cell, e.g., a T cell, by transducing the cell with anadeno-associated virus (AAV), retrovirus, e.g., lentivirus, IDLY, etc.,herpes simplex virus, adenovirus, or vaccinia virus vector comprisingthe donor repair template.

In particular embodiments, the donor repair template comprises one ormore homology arms that flank the DSB site.

As used herein, the term “homology arms” refers to a nucleic acidsequence in a donor repair template that is identical, or nearlyidentical, to DNA sequence flanking the DNA break introduced by thenuclease at a target site. In one embodiment, the donor repair templatecomprises a 5′ homology arm that comprises a nucleic acid sequence thatis identical or nearly identical to the DNA sequence 5′ of the DNA breaksite. In one embodiment, the donor repair template comprises a 3′homology arm that comprises a nucleic acid sequence that is identical ornearly identical to the DNA sequence 3′ of the DNA break site. In apreferred embodiment, the donor repair template comprises a 5′ homologyarm and a 3′ homology arm. The donor repair template may comprisehomology to the genome sequence immediately adjacent to the DSB site, orhomology to the genomic sequence within any number of base pairs fromthe DSB site. In particular embodiments, a pair of homology armscomprises a homology arm comprising a polynucleotide sequence thatincludes a target site for a double strand break with a mutation in thetarget site to minimize re-cleavage of the target site. In oneembodiment, the donor repair template comprises a nucleic acid sequencethat is homologous to a genomic sequence or homology arm of about 5 bp,about 10 bp, about 25 bp, about 50 bp, about 100 bp, about 250 bp, about500 bp, about 1000 bp, about 2500 bp, about 5000 bp, about 10000 bp ormore, including any intervening length of homologous sequence.

Illustrative examples of suitable lengths of homology arms contemplatedin particular embodiments, may be independently selected, and includebut are not limited to: 5 bp, about 10 bp, about 25 bp, about 50 bp,about 100 bp, about 200 bp, about 300 bp, about 400 bp, about 500 bp,about 600 bp, about 700 bp, about 800 bp, about 900 bp, about 1000 bp,about 1100 bp, about 1200 bp, about 1300 bp, about 1400 bp, about 1500bp, about 1600 bp, about 1700 bp, about 1800 bp, about 1900 bp, about2000 bp, about 2100 bp, about 2200 bp, about 2300 bp, about 2400 bp,about 2500 bp, about 2600 bp, about 2700 bp, about 2800 bp, about 2900bp, or about 3000 bp, or longer homology arms, including all interveninglengths of homology arms.

Additional illustrative examples of suitable homology arm lengthsinclude, but are not limited to: about 100 bp to about 3000 bp, about200 bp to about 3000 bp, about 300 bp to about 3000 bp, about 400 bp toabout 3000 bp, about 500 bp to about 3000 bp, about 500 bp to about 2500bp, about 500 bp to about 2000 bp, about 750 bp to about 2000 bp, about750 bp to about 1500 bp, or about 1000 bp to about 1500 bp, includingall intervening lengths of homology arms.

In a particular embodiment, the lengths of the 5′ and 3′ homology armsare independently selected from about 500 bp to about 1500 bp. In oneembodiment, the 5′homology arm is about 1500 bp and the 3′ homology armis about 1000 bp. In one embodiment, the 5′homology arm is between about200 bp to about 600 bp and the 3′ homology arm is between about 200 bpto about 600 bp. In one embodiment, the 5′homology arm is about 200 bpand the 3′ homology arm is about 200 bp. In one embodiment, the5′homology arm is about 300 bp and the 3′ homology arm is about 300 bp.In one embodiment, the 5′homology arm is about 400 bp and the 3′homology arm is about 400 bp. In one embodiment, the 5′homology arm isabout 500 bp and the 3′ homology arm is about 500 bp. In one embodiment,the 5′homology arm is about 600 bp and the 3′ homology arm is about 600bp.

Donor repair templates may comprise one or more expression cassettes inparticular embodiments. In certain embodiments, donor repair templatesmay comprise one or homology arms and one or more polynucleotidesincluding, but not limited to promoters and/or enhancers, untranslatedregions (UTRs), Kozak sequences, polyadenylation signals, additionalrestriction enzyme sites, multiple cloning sites, internal ribosomalentry sites (IRES), recombinase recognition sites (e.g., LoxP, FRT, andAtt sites), termination codons, transcriptional termination signals,polynucleotides encoding self-cleaving polypeptides, and epitope tags.

In various embodiments, the donor repair template comprises a 5′homology arm, an RNA polymerase II promoter, one or more polynucleotidesencoding an immunopotency enhancer, an immunosuppressive signal damper,or an engineered antigen receptor, and a 3′ homology arm.

In various embodiments, a target site is modified with a donor repairtemplate comprising a 5′ homology arm, one or more polynucleotidesencoding self-cleaving viral peptide, e.g., T2A, an immunopotencyenhancer, an immunosuppressive signal damper, or an engineered antigenreceptor, optionally a poly(A) signal or self-cleaving peptide, and a 3′homology arm, wherein expression of the one or more polynucleotides isgoverned by the endogenous CBLB promoter.

1. Immunopotency Enhancers

In particular embodiments, the genome edited immune effector cellscontemplated herein are made more potent and/or resistant toimmunosuppressive factors by introducing a DSB in the CBLB gene in thepresence of a donor repair template comprising a polynucleotide encodingan immunopotency enhancer. As used herein, the term “immunopotencyenhancer” refers to non-naturally occurring molecules that stimulateand/or potentiate T cell activation and/or function, immunopotentiatingfactors, and non-naturally occurring polypeptides that convert theimmunosuppressive signals from the tumor microenvironment to animmunostimulatory signal in a T cell or other immune cells.

In particular embodiments, the immunopotency enhancer is selected fromthe group consisting of: a bispecific T cell engager (BilE) molecule; animmunopotentiating factor including, but not limited to, cytokines,chemokines, cytotoxins, and/or cytokine receptors; and a flip receptor.

In some embodiments, the immunopotency enhancer, immunopotentiatingfactor, or flip receptor are fusion polypeptides comprising a proteindestabilization domain.

a. Bispecific T Cell Engager (BiTE) Molecules

In particular embodiments, the genome edited immune effector cellscontemplated herein are made more potent by introducing a DSB in theCBLB gene in the presence of a donor repair template comprising apolynucleotide encoding a bispecific T cell engager (BiTE) molecules.BiTE molecules are bipartite molecules comprising a first binding domainthat binds a target antigen, a linker or spacer as contemplatedelsewhere herein, and a second binding domain that binds a stimulatoryor costimulatory molecule on an immune effector cell. The first andsecond binding domains may be independently selected from ligands,receptors, antibodies or antigen binding fragments thereof, lectins, andcarbohydrates.

In particular embodiments, the first and second binding domains areantigen binding domains.

In particular embodiments, the first and second binding domains areantibodies or antigen binding fragments thereof. In one embodiment, thefirst and second binding domains are single chain variable fragments(scFv).

Illustrative examples of target antigens that may be recognized andbound by the first binding domain in particular embodiments include, butare not limited to: alpha folate receptor, 5T4, αvβ6 integrin, BCMA,B7-H3, B7-H6, CAIX, CD16, CD19, CD20, CD22, CD30, CD33, CD44, CD44v6,CD44v7/8, CD70, CD79a, CD79b, CD123, CD138, CD171, CEA, CSPG4, EGFR,EGFR family including ErbB2 (HER2), EGFRvIII, EGP2, EGP40, EPCAM, EphA2,EpCAM, FAP, fetal AchR, GD2, GD3, Glypican-3 (GPC3), HLA-A1+MAGE1,HLA-A2+MAGE1, HLA-A3+MAGE1, HLA-A1+NY-ESO-1, HLA-A2+NY-ESO-1,HLA-A3+NY-ESO-1, IL-11Rα, IL-13Rα2, Lambda, Lewis-Y, Kappa, Mesothelin,Muc1, Muc16, NCAM, NKG2D Ligands, NY-ESO-1, PRAME, PSCA, PSMA, ROR1,SSX, Survivin, TAG72, TEMs, VEGFR2, and WT-1.

Other illustrative embodiments of target antigens include MHC-peptidecomplexes, optionally wherein the peptide is processed from: alphafolate receptor, 5T4, αvβ6 integrin, BCMA, B7-H3, B7-H6, CAIX, CD16,CD19, CD20, CD22, CD30, CD33, CD44, CD44v6, CD44v7/8, CD70, CD79a,CD79b, CD123, CD138, CD171, CEA, CSPG4, EGFR, EGFR family includingErbB2 (HER2), EGFRvIII, EGP2, EGP40, EPCAM, EphA2, EpCAM, FAP, fetalAchR, GD2, GD3, Glypican-3 (GPC3), MAGE1, NY-ESO-1, IL-11Rα, IL-13Rα2,Lambda, Lewis-Y, Kappa, Mesothelin, Muc1, Muc16, NCAM, NKG2D Ligands,PRAME, PSCA, PSMA, ROR1, SSX, Survivin, TAG72, TEMs, VEGFR2, and WT-1.

Illustrative examples of stimulatory or co-stimulatory molecules onimmune effector cells recognized and bound by the second binding domainin particular embodiments include, but are not limited to: CD3γ, CD3δ,CD3ε, CD3ζ, CD28, CD134, CD137, and CD278.

In particular embodiments, a DSB is induced in a CBLB gene by anengineered nuclease, and a donor repair template comprising apolynucleotide encoding a BiTE is introduced into the cell and isinserted into the CBLB gene by homologous recombination.

b. Immunopotentiating Factors

In particular embodiments, the genome edited immune effector cellscontemplated herein are made more potent by increasingimmunopotentiating factors either in the genome edited cells or cells inthe tumor microenvironment. Immunopotentiating factors refer toparticular cytokines, chemokines, cytoxins, and cytokine receptors thatpotentiate the immune response in immune effector cells. In oneembodiment, T cells are engineered by introducing a DSB in the CBLB genein the presence of a donor repair template comprising a polynucleotideencoding a cytokine, chemokine, cytotoxin, or cytokine receptor.

In particular embodiments, the donor repair template comprises apolynucleotide encoding a cytokine selected from the group consistingof: IL-2, insulin, IFN-γ, IL-7, IL-21, IL-10, IL-12, IL-15, and TNF-α.

In particular embodiments, the donor repair template comprises apolynucleotide encoding a chemokine selected from the group consistingof: MIP-1α, MIP-1β, MCP-1, MCP-3, and RANTES.

In particular embodiments, the donor repair template comprises apolynucleotide encoding a cytotoxin selected from the group consistingof: Perforin, Granzyme A, and Granzyme B.

In particular embodiments, the donor repair template comprises apolynucleotide encoding a cytokine receptor selected from the groupconsisting of: an IL-2 receptor, an IL-7 receptor, an IL-12 receptor, anIL-15 receptor, and an IL-21 receptor.

c. Flip Receptors

In particular embodiments, the genome edited immune effector cellscontemplated herein are made more resistant to exhaustion by “flipping”or “reversing” the immunosuppressive signal by immunosuppressive factorselicited by the tumor microenvironment to a positive immunostimulatorysignal. In one embodiment, T cells are engineered by introducing a DSBinto a CBLB gene in the presence of a donor repair template comprising apolynucleotide encoding a flip receptor. As used herein, the term “flipreceptor” refers to a non-naturally occurring polypeptide that convertsthe immunosuppressive signals from the tumor microenvironment to animmunostimulatory signal in a T cell. In preferred embodiments, a flipreceptor refers to a polypeptide that comprises an exodomain that bindsan immunosuppressive factor, a transmembrane domain, and an endodomainthat transduces an immunostimulatory signal to a T cell.

In one embodiment, the donor repair template encodes a flip receptorcomprising an exodomain or extracellular binding domain that binds animmunosuppressive cytokine, a transmembrane domain, and an endodomain ofan immunopotentiating cytokine receptor.

In particular embodiments, a flip receptor comprises an exodomain thatbinds an immunosuppressive cytokine is the extracellular cytokinebinding domain of an IL-4 receptor, IL-6 receptor, IL-8 receptor, IL-10receptor, IL-13 receptor, TGFβ receptor 1, or TGFβ receptor 2; atransmembrane isolated from CD4, CD8α, CD27, CD28, CD134, CD137, CD3,TGFβ receptor 1, TGFβ receptor 2, IL-2 receptor, IL-7 receptor, IL-12receptor, IL-15 receptor, or IL-21 receptor; and an endodomain isolatedfrom an IL-2 receptor, IL-7 receptor, IL-12 receptor, IL-15 receptor, orIL-21 receptor.

In particular embodiments, a flip receptor comprises an exodomain thatbinds an immunosuppressive cytokine is an antibody or antigen bindingfragment thereof that binds IL-4, IL-6, IL-8, IL-10, IL-13, TGFβreceptor 1, or TGFβ receptor 2; a transmembrane isolated from CD4, CD8a,CD27, CD28, CD134, CD137, a CD3, TGFβ receptor 1, or TGFβ receptor 2,IL-2 receptor, IL-7 receptor, IL-12 receptor, IL-15 receptor, or IL-21receptor; and an endodomain isolated from an IL-2 receptor, IL-7receptor, IL-12 receptor, IL-15 receptor, or IL-21 receptor.

In one embodiment, the donor repair template comprises a flip receptorcomprising an exodomain that binds an immunosuppressive factor, atransmembrane domain, and one or more intracellular co-stimulatorysignaling domains and/or primary signaling domains.

Illustrative examples of exodomains suitable for use in particularembodiments of flip receptors contemplated in particular embodimentsinclude, but are not limited to: an extracellular ligand binding domainof a receptor that comprises an ITIM and/or an ITSM.

Further illustrative examples of exodomains suitable for use inparticular embodiments of flip receptors contemplated in particularembodiments include, but are not limited to an extracellular ligandbinding domain of: PD-1, LAG-3, TIM-3, CTLA-4, BTLA, CEACAM1, TIGIT,TGFβRI, TGFβRII, IL4R, IL6R, CXCR1, CXCR2, IL10R, IL13Rα2, TRAILR1,RCAS1R, and FAS.

In one embodiment, the exodomain comprises an extracellular ligandbinding domain of a receptor selected from the group consisting of:PD-1, LAG-3, TIM-3, CTLA-4, IL10R, TIGIT, TGFβRI, and TGFβRII.

In one embodiment, the donor repair template comprises a flip receptorcomprising an exodomain that binds an immunosuppressive cytokine, atransmembrane domain, and one or more intracellular co-stimulatorysignaling domains and/or primary signaling domains.

Illustrative examples of transmembrane domains suitable for use inparticular embodiments of flip receptors contemplated in particularembodiments include, but are not limited to transmembrane domains of thefollowing proteins: PD-1, LAG-3, TIM-3, CTLA-4, IL10R, TIGIT, TGFβRI andTGFβRII alpha or beta chain of the T-cell receptor, CDδ, CD3ε, CDγ,CD3ζ, CD4, CD5, CD8α, CD9, CD 16, CD22, CD27, CD28, CD33, CD37, CD45,CD64, CD80, CD86, CD 134, CD137, or CD154.

In various embodiments, the flip receptor comprises an endodomain thatelicits an immunostimulatory signal. As used herein, the term“endodomain” refers to an immunostimulatory motif or domain, includingbut not limited to an immunoreceptor tyrosine activation motif (ITAM), acostimulatory signaling domain, a primary signaling domain, or anotherintracellular domain that is associated with eliciting immunostimulatorysignals in T cells.

Illustrative examples of endodomains suitable for use in particularembodiments of flip receptors contemplated in particular embodimentsinclude, but are not limited to domains comprising an ITAM motif.

Additional illustrative examples of endodomains suitable for use inparticular embodiments of flip receptors contemplated in particularembodiments include, but are not limited to co-stimulatory signalingdomains is isolated from: TLR1, TLR2, TLR3, TLR4, TLR5, TLR6, TLR7,TLR8, TLR9, TLR10, CARD11, CD2, CD7, CD27, CD28, CD30, CD40, CD54(ICAM), CD83, CD134 (OX40), CD137 (4-1BB), CD278 (ICOS), DAP10, LAT,NKD2C, SLP76, TRIM, or ZAP70.

Additional illustrative examples of endodomains suitable for use inparticular embodiments of flip receptors contemplated in particularembodiments include, but are not limited to: an endodomain isolated froman IL-2 receptor, IL-7 receptor, IL-12 receptor, IL-15 receptor, orIL-21 receptor.

Further illustrative examples of endodomains suitable for use inparticular embodiments of flip receptors contemplated in particularembodiments include, but are not limited to primary signaling domains isisolated from: FcRγ, FcRβ, CD3γ, CD3δ, CD3ε, CD3ζ, CD22, CD79a, CD79b,and CD66d.

In particular embodiments, the flip receptor comprises an exodomain thatcomprises an extracellular domain from PD-1, LAG-3, TIM-3, CTLA-4,IL10R, TIGIT, TGFβRI or TGFβRII: an endodomain isolated from an IL-2receptor, IL-7 receptor, IL-12 receptor, IL-15 receptor, or IL-21receptor.

In particular embodiments, the flip receptor comprises an exodomain thatcomprises an extracellular domain from PD-1, LAG-3, TIM-3, CTLA-4,IL10R, TIGIT, TGFβRI or TGFβRII; a transmembrane domain from a CD3polypeptide, CD4, CD8α, CD28, CD134, CD137, PD-1, LAG-3, TIM-3, CTLA-4,IL10R, TGFβRI and TGFβRII; and an endodomain from CD28, CD134, CD137,CD278, and/or CD3ζ.

In particular embodiments, the flip receptor comprises an exodomain thatcomprises an extracellular domain from PD-1, LAG-3, TIM-3, CTLA-4,IL10R, TIGIT, or TGFβRII; a transmembrane domain from a CD3 polypeptide,CD4, CD8α, CD28, CD134, or CD137; and an endodomain from CD28, CD134,CD137, CD278, and/or CD3ζ.

2. Immunosuppressive Signal Dampers

One limitation or problem that vexes existing adoptive cell therapy ishyporesponsiveness of immune effector cells due to exhaustion mediatedby the tumor microenvironment. Exhausted T cells have a unique molecularsignature that is markedly distinct from naive, effector or memory Tcells. They are defined as T cells with decreased cytokine expressionand effector function.

In particular embodiments, genome edited immune effector cellscontemplated herein are made more resistant to exhaustion by decreasingor damping signaling by immunosuppressive factors. In one embodiment, Tcells are engineered by introducing a DSB in the CBLB gene in thepresence of a donor repair template comprising a polynucleotide encodingan immunosuppressive signal damper.

As used herein, the term “immunosuppressive signal damper” refers to anon-naturally occurring polypeptide that decreases the transduction ofimmunosuppressive signals from the tumor microenvironment to a T cell.In one embodiment, the immunosuppressive signal damper is an antibody orantigen binding fragment thereof that binds an immunosuppressive factor.In preferred embodiments, an immunosuppressive signal damper refers to apolypeptide that elicits a suppressive, dampening, or dominant negativeeffect on a particular immunosuppressive factor or signaling pathwaybecause the damper comprises and exodomain that binds animmunosuppressive factor, and optionally, a transmembrane domain, andoptionally, a modified endodomain (e.g., intracellular signalingdomain).

In particular embodiments, the exodomain is an extracellular bindingdomain that recognizes and binds and immunosuppressive factor.

In particular embodiments, the modified endodomain is mutated todecrease or inhibit immunosuppressive signals. Suitable mutationstrategies include, but are not limited to amino acid substitution,addition, or deletion. Suitable mutations further include, but are notlimited to endodomain truncation to remove signaling domains, mutatingendodomains to remove residues important for signaling motif activity,and mutating endodomains to block receptor cycling. In particularembodiments, the endodomain, when present does not transduceimmunosuppressive signals, or has substantially reduced signaling.

Thus, in some embodiments, an immunosuppressive signal damper acts assink for one or more immunosuppressive factors from the tumormicroenvironment and inhibits the corresponding immunosuppressivesignaling pathways in the T cell.

One immunosuppressive signal is mediated by tryptophan catabolism.Tryptophan catabolism by indoleamine 2,3-dioxygenase (IDO) in cancercells leads to the production of kynurenines which have been shown tohave an immunosuppressive effect on T cells in the tumormicroenvironment. See e.g., Platten et al. (2012) Cancer Res.72(21):5435-40.

In one embodiment, a donor repair template comprises an enzyme withkynureninase activity.

Illustrative examples of enzymes having kynureninase activity suitablefor use in particular embodiments include, but are not limited to,L-Kynurenine hydrolase.

In one embodiment, the donor repair template comprises one or morepolynucleotides that encodes an immunosuppressive signal damper thatdecrease or block immunosuppressive signaling mediated by animmunosuppressive factor.

Illustrative examples of immunosuppressive factors targeted by theimmunosuppressive signal dampers contemplated in particular embodimentsinclude, but are not limited to: programmed death ligand 1 (PD-L1),programmed death ligand 2 (PD-L2), transforming growth factor β (TGFβ),macrophage colony-stimulating factor 1 (M-CSF1), tumor necrosis factorrelated apoptosis inducing ligand (TRAIL), receptor-binding cancerantigen expressed on SiSo cells ligand (RCAS1), Fas ligand (FasL), CD47,interleukin-4 (IL-4), interleukin-6 (IL-6), interleukin-8 (IL-8),interleukin-10 (IL-10), and interleukin-13 (IL-13).

In various embodiments, the immunosuppressive signal damper comprises anantibody or antigen binding fragment thereof that binds animmunosuppressive factor.

In various embodiments, the immunosuppressive signal damper comprises anexodomain that binds an immunosuppressive factor.

In particular embodiments, the immunosuppressive signal damper comprisesan exodomain that binds an immunosuppressive factor and a transmembranedomain.

In another embodiment, the immunosuppressive signal damper comprises anexodomain that binds an immunosuppressive factor, a transmembranedomain, and a modified endodomain that does not transduce or that hassubstantially reduced ability to transduce immunosuppressive signals.

As used herein, the term “exodomain” refers to an antigen bindingdomain. In one embodiment, the exodomain is an extracellular ligandbinding domain of an immunosuppressive receptor that transducesimmunosuppressive signals from the tumor microenvironment to a T cell.In particular embodiments, an exodomain refers to an extracellularligand binding domain of a receptor that comprises an immunoreceptortyrosine inhibitory motif (ITIM) and/or an immunoreceptor tyrosineswitch motif (ITSM).

Illustrative examples of exodomains suitable for use in particularembodiments of immunosuppressive signal dampers include, but are notlimited to antibodies or antigen binding fragments thereof, orextracellular ligand binding domains isolated from the followingpolypeptides: programmed cell death protein 1 (PD-1), lymphocyteactivation gene 3 protein (LAG-3), T cell immunoglobulin domain andmucin domain protein 3 (TIM3), cytotoxic T lymphocyte antigen-4(CTLA-4), band T lymphocyte attenuator (BTLA), T cell immunoglobulin andimmunoreceptor tyrosine-based inhibitory motif domain (TIGIT),transforming growth factor β receptor 1 (TGFβRI), transforming growthfactor β receptor 2 (TGFβRII), macrophage colony-stimulating factor 1receptor (CSF1R), interleukin 4 receptor (IL4R), interleukin 6 receptor(IL6R), chemokine (C-X-C motif) receptor 1 (CXCR1), chemokine (C-X-Cmotif) receptor 2 (CXCR2), interleukin 10 receptor subunit alpha(IL10R), interleukin 13 receptor subunit alpha 2 (IL13Rα2), tumornecrosis factor related apoptosis inducing ligand (TRAILR1),receptor-binding cancer antigen expressed on SiSo cells (RCAS1R), andFas cell surface death receptor (FAS).

In one embodiment, the exodomain comprises an extracellular ligandbinding domain of a receptor selected from the group consisting of:PD-1, LAG-3, TIM3, CTLA-4, IL10R, TIGIT, CSF1R, TGFβRII and TGFβRII.

A number of transmembrane domains may be used in particular embodiments.Illustrative examples of transmembrane domains suitable for use inparticular embodiments of immunosuppressive signal dampers contemplatedin particular embodiments include, but are not limited to transmembranedomains of the following proteins: alpha or beta chain of the T-cellreceptor, CDδ, CD3ε, CDγ, CD3ζ, CD4, CD5, CD8α, CD9, CD 16, CD22, CD27,CD28, CD33, CD37, CD45, CD64, CD80, CD86, CD 134, CD137, CD152, CD154,and PD-1.

3. Engineered Antigen Receptors

In particular embodiments, the genome edited immune effector cellscontemplated herein comprise an engineered antigen receptor. In oneembodiment, T cells comprising a polynucleotide encoding an engineeredantigen receptor are edited by introducing a DSB in a CBLB gene. In oneembodiment, T cells are engineered by introducing a DSB in a CBLB genein the presence of a donor repair template comprising a polynucleotideencoding an engineered antigen receptor.

In particular embodiments, the engineered antigen receptor is anengineered T cell receptor (TCR), a chimeric antigen receptor (CAR), aDaric receptor or components thereof, or a chimeric cytokine receptor.

a. Engineered TCRs

In particular embodiments, the genome edited immune effector cellscontemplated herein comprise a polynucleotide encoding an engineeredTCR. In one embodiment, T cells comprising a polynucleotide encoding anengineered TCR are edited by introducing a DSB in a CBLB gene. In oneembodiment, T cells are engineered by introducing a DSB in a CBLB genein the presence of a donor repair template encoding an engineered TCR.In a particular embodiment, an engineered TCR is inserted at a DSB in asingle CBLB allele. Another embodiment, the alpha chain of an engineeredTCR is inserted into a DSB in one CBLB allele and the beta chain of theengineered TCR is inserted into a DSB in the other CBLB allele.

In one embodiment, the engineered T cells contemplated herein comprise apolynucleotide encoding an engineered TCR that is not inserted at a CBLBgene and/or one or more of an immunosuppressive signal damper, a flipreceptor, an alpha and/or beta chain of an engineered T cell receptor(TCR), a chimeric antigen receptor (CAR), a Daric receptor or componentsthereof, or a chimeric cytokine receptor is inserted into a DSB in oneor more CBLB alleles.

Naturally occurring T cell receptors comprise two subunits, an alphachain and a beta chain subunit, each of which is a unique proteinproduced by recombination event in each T cell's genome. Libraries ofTCRs may be screened for their selectivity to particular targetantigens. In this manner, natural TCRs, which have a high-avidity andreactivity toward target antigens may be selected, cloned, andsubsequently introduced into a population of T cells used for adoptiveimmunotherapy.

In one embodiment, T cells are modified by introducing donor repairtemplate comprising a polynucleotide encoding a subunit of a TCR at aDSB in one or more CBLB alleles, wherein the TCR subunit has the abilityto form TCRs that confer specificity to T cells for tumor cellsexpressing a target antigen. In particular embodiments, the subunitshave one or more amino acid substitutions, deletions, insertions, ormodifications compared to the naturally occurring subunit, so long asthe subunits retain the ability to form TCRs and confer upon transfectedT cells the ability to home to target cells, and participate inimmunologically-relevant cytokine signaling. The engineered TCRspreferably also bind target cells displaying the relevanttumor-associated peptide with high avidity, and optionally mediateefficient killing of target cells presenting the relevant peptide invivo.

The nucleic acids encoding engineered TCRs are preferably isolated fromtheir natural context in a (naturally-occurring) chromosome of a T cell,and can be incorporated into suitable vectors as described elsewhereherein. Both the nucleic acids and the vectors comprising them can betransferred into a cell, preferably a T cell in particular embodiments.The modified T cells are then able to express one or more chains of aTCR encoded by the transduced nucleic acid or nucleic acids. Inpreferred embodiments, the engineered TCR is an exogenous TCR because itis introduced into T cells that do not normally express the particularTCR. The essential aspect of the engineered TCRs is that it has highavidity for a tumor antigen presented by a major histocompatibilitycomplex (MHC) or similar immunological component. In contrast toengineered TCRs, CARs are engineered to bind target antigens in an MHCindependent manner.

The TCR can be expressed with additional polypeptides attached to theamino-terminal or carboxyl-terminal portion of the inventive alpha chainor beta chain of a TCR so long as the attached additional polypeptidedoes not interfere with the ability of the alpha chain or beta chain toform a functional T cell receptor and the MHC dependent antigenrecognition.

Antigens that are recognized by the engineered TCRs contemplated inparticular embodiments include, but are not limited to cancer antigens,including antigens on both hematological cancers and solid tumors.Illustrative antigens include, but are not limited to alpha folatereceptor, 5T4, αvβ6 integrin, BCMA, B7-H3, B7-H6, CAIX, CD19, CD20,CD22, CD30, CD33, CD44, CD44v6, CD44v7/8, CD70, CD79a, CD79b, CD123,CD138, CD171, CEA, CSPG4, EGFR, EGFR family including ErbB2 (HER2),EGFRvlI, EGP2, EGP40, EPCAM, EphA2, EpCAM, FAP, fetal AchR, GD2, GD3,Glypican-3 (GPC3), HLA-A1+MAGE1, HLA-A2+MAGE1, HLA-A3+MAGE1,HLA-A1+NY-ESO-1, HLA-A2+NY-ESO-1, HLA-A3+NY-ESO-1, IL-11Rα, IL-13Rα2,Lambda, Lewis-Y, Kappa, Mesothelin, Muc1, Muc16, NCAM, NKG2D Ligands,NY-ESO-1, PRAME, PSCA, PSMA, ROR1, SSX, Survivin, TAG72, TEMs, VEGFR2,and WT-1.

In one embodiment, a donor repair template comprises a polynucleotideencoding an RNA polymerase II promoter or a first self-cleaving viralpeptide and a polynucleotide encoding the alpha chain and/or the betachain of the engineered TCR integrated into one modified and/ornon-functional CBLB gene.

In one embodiment, a donor repair template comprises a polynucleotideencoding an RNA polymerase II promoter or a first self-cleaving viralpeptide and a polynucleotide encoding the alpha chain and the beta chainof the engineered TCR integrated into one modified and/or non-functionalCBLB gene.

In a particular embodiment, the donor repair template comprises from 5′to 3′, a polynucleotide encoding a first self-cleaving viral peptide, apolynucleotide encoding the alpha chain of the engineered TCR, apolynucleotide encoding a second self-cleaving viral peptide, and apolynucleotide encoding the beta chain of the engineered TCR integratedinto one modified and/or non-functional CBLB gene. In such a case, theother CBLB gene may be functional or may have decreased function or beenrendered non-functional by a DSB and repair by NHEJ. In one embodiment,the other CBLB gene has been modified by an engineered nucleasecontemplated herein and may have decreased function or been renderednon-functional.

In a certain embodiment, both CBLB genes are modified and have decreasedfunction or are non-functional: the first modified CBLB gene comprises anucleic acid comprising a polynucleotide encoding a first self-cleavingviral peptide and a polynucleotide encoding the alpha chain of theengineered TCR, and the second modified CBLB gene comprises apolynucleotide encoding a second self-cleaving viral peptide and apolynucleotide encoding the beta chain of the engineered TCR.

b. Chimeric Antigen Receptors (CARs)

In particular embodiments, the engineered immune effector cellscontemplated herein comprise one or more chimeric antigen receptors(CARs). In one embodiment, T cells comprising a polynucleotide encodingone or more CARs are edited by introducing a DSB in a CBLB gene. In oneembodiment, T cells are engineered by introducing a DSB in one or moreCBLB genes in the presence of a donor repair template encoding a CAR. Ina particular embodiment, a CAR is inserted at a DSB in a single CBLBgene.

In one embodiment, the engineered T cells contemplated herein a CAR thatis not inserted at a CBLB gene and one or more of an immunosuppressivesignal damper, a flip receptor, an alpha and/or beta chain of anengineered T cell receptor (TCR), a chimeric antigen receptor (CAR), aDaric receptor or components thereof, or a chimeric cytokine receptor isinserted into a DSB in one or more CBLB genes.

In various embodiments, the genome edited T cells express CARs thatredirect cytotoxicity toward tumor cells. CARs are molecules thatcombine antibody-based specificity for a target antigen (e.g., tumorantigen) with a T cell receptor-activating intracellular domain togenerate a chimeric protein that exhibits a specific anti-tumor cellularimmune activity. As used herein, the term, “chimeric,” describes beingcomposed of parts of different proteins or DNAs from different origins.

In various embodiments, a CAR comprises an extracellular domain thatbinds to a specific target antigen (also referred to as a binding domainor antigen-specific binding domain), a transmembrane domain and anintracellular signaling domain. The main characteristic of CARs aretheir ability to redirect immune effector cell specificity, therebytriggering proliferation, cytokine production, phagocytosis orproduction of molecules that can mediate cell death of the targetantigen expressing cell in a major histocompatibility (MHC) independentmanner, exploiting the cell specific targeting abilities of monoclonalantibodies, soluble ligands or cell specific coreceptors.

In particular embodiments, CARs comprise an extracellular binding domainthat specifically binds to a target polypeptide, e.g., target antigen,expressed on tumor cell. As used herein, the terms, “binding domain,”“extracellular domain,” “extracellular binding domain,” “antigen bindingdomain,” “antigen-specific binding domain,” and “extracellular antigenspecific binding domain,” are used interchangeably and provide achimeric receptor, e.g., a CAR or Daric, with the ability tospecifically bind to the target antigen of interest. A binding domainmay comprise any protein, polypeptide, oligopeptide, or peptide thatpossesses the ability to specifically recognize and bind to a biologicalmolecule (e.g., a cell surface receptor or tumor protein, lipid,polysaccharide, or other cell surface target molecule, or componentthereof). A binding domain includes any naturally occurring, synthetic,semi-synthetic, or recombinantly produced binding partner for abiological molecule of interest.

In particular embodiments, the extracellular binding domain comprises anantibody or antigen binding fragment thereof.

An “antibody” refers to a binding agent that is a polypeptide comprisingat least a light chain or heavy chain immunoglobulin variable regionwhich specifically recognizes and binds an epitope of a target antigen,such as a peptide, lipid, polysaccharide, or nucleic acid containing anantigenic determinant, such as those recognized by an immune cell.Antibodies include antigen binding fragments, e.g., Camel Ig (a camelidantibody or VHH fragment thereof), Ig NAR, Fab fragments, Fab′fragments, F(ab)′2 fragments, F(ab)′3 fragments, Fv, single chain Fvantibody (“scFv”), bis-scFv, (scFv)2, minibody, diabody, triabody,tetrabody, disulfide stabilized Fv protein (“dsFv”), and single-domainantibody (sdAb, Nanobody) or other antibody fragments thereof. The termalso includes genetically engineered forms such as chimeric antibodies(for example, humanized murine antibodies), heteroconjugate antibodies(such as, bispecific antibodies) and antigen binding fragments thereof.See also, Pierce Catalog and Handbook, 1994-1995 (Pierce Chemical Co.,Rockford, Ill.); Kuby, J., Immunology, 3rd Ed., W. H. Freeman & Co., NewYork, 1997.

In one preferred embodiment, the binding domain is an scFv.

In another preferred embodiment, the binding domain is a camelidantibody.

In particular embodiments, the CAR comprises an extracellular domainthat binds an antigen selected from the group consisting of: alphafolate receptor, 5T4, αvβ6 integrin, BCMA, B7-H3, B7-H6, CAIX, CD16,CD19, CD20, CD22, CD30, CD33, CD44, CD44v6, CD44v7/8, CD70, CD79a,CD79b, CD123, CD138, CD171, CEA, CSPG4, EGFR, EGFR family includingErbB2 (HER2), EGFRvIII, EGP2, EGP40, EPCAM, EphA2, EpCAM, FAP, fetalAchR, GD2, GD3, Glypican-3 (GPC3), HLA-A1+MAGEL HLA-A2+MAGE1,HLA-A3+MAGE1, HLA-A1+NY-ESO-1, HLA-A2+NY-ESO-1, HLA-A3+NY-ESO-1,IL-11Rα, IL-13Rα2, Lambda, Lewis-Y, Kappa, Mesothelin, Muc1, Muc16,NCAM, NKG2D Ligands, NY-ESO-1, PRAME, PSCA, PSMA, ROR1, SSX, Survivin,TAG72, TEMs, VEGFR2, and WT-1.

In particular embodiments, the CARs comprise an extracellular bindingdomain, e.g., antibody or antigen binding fragment thereof that binds anantigen, wherein the antigen is an MHC-peptide complex, such as a classI MHC-peptide complex or a class II MHC-peptide complex.

In certain embodiments, the CARs comprise linker residues between thevarious domains. A “variable region linking sequence,” is an amino acidsequence that connects a heavy chain variable region to a light chainvariable region and provides a spacer function compatible withinteraction of the two sub-binding domains so that the resultingpolypeptide retains a specific binding affinity to the same targetmolecule as an antibody that comprises the same light and heavy chainvariable regions. In particular embodiments, CARs comprise one, two,three, four, or five or more linkers. In particular embodiments, thelength of a linker is about 1 to about 25 amino acids, about 5 to about20 amino acids, or about 10 to about 20 amino acids, or any interveninglength of amino acids. In some embodiments, the linker is 1, 2, 3, 4, 5,6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24,25, or more amino acids long.

In particular embodiments, the binding domain of the CAR is followed byone or more “spacer domains,” which refers to the region that moves theantigen binding domain away from the effector cell surface to enableproper cell/cell contact, antigen binding and activation (Patel et al.,Gene Therapy, 1999; 6: 412-419). The spacer domain may be derived eitherfrom a natural, synthetic, semi-synthetic, or recombinant source. Incertain embodiments, a spacer domain is a portion of an immunoglobulin,including, but not limited to, one or more heavy chain constant regions,e.g., CH2 and CH3. The spacer domain can include the amino acid sequenceof a naturally occurring immunoglobulin hinge region or an alteredimmunoglobulin hinge region.

In one embodiment, the spacer domain comprises the CH2 and CH3 of IgG1,IgG4, or IgD.

In one embodiment, the binding domain of the CAR is linked to one ormore “hinge domains,” which plays a role in positioning the antigenbinding domain away from the effector cell surface to enable propercell/cell contact, antigen binding and activation. A CAR generallycomprises one or more hinge domains between the binding domain and thetransmembrane domain (TM). The hinge domain may be derived either from anatural, synthetic, semi-synthetic, or recombinant source. The hingedomain can include the amino acid sequence of a naturally occurringimmunoglobulin hinge region or an altered immunoglobulin hinge region.

Illustrative hinge domains suitable for use in the CARs described hereininclude the hinge region derived from the extracellular regions of type1 membrane proteins such as CD8α, and CD4, which may be wild-type hingeregions from these molecules or may be altered. In another embodiment,the hinge domain comprises a CD8α hinge region.

In one embodiment, the hinge is a PD-1 hinge or CD152 hinge.

The “transmembrane domain” is the portion of the CAR that fuses theextracellular binding portion and intracellular signaling domain andanchors the CAR to the plasma membrane of the immune effector cell. TheTM domain may be derived either from a natural, synthetic,semi-synthetic, or recombinant source.

Illustrative TM domains may be derived from (i.e., comprise at least thetransmembrane region(s) of the alpha or beta chain of the T-cellreceptor, CD3δ, CD3ε, CD3γ, CD3ζ, CD4, CD5, CD8α, CD9, CD 16, CD22,CD27, CD28, CD33, CD37, CD45, CD64, CD80, CD86, CD 134, CD137, CD152,CD154, AMN, and PD-1.

In one embodiment, a CAR comprises a TM domain derived from CD8α. Inanother embodiment, a CAR contemplated herein comprises a TM domainderived from CD8α and a short oligo- or polypeptide linker, preferablybetween 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 amino acids in length thatlinks the TM domain and the intracellular signaling domain of the CAR. Aglycine-serine linker provides a particularly suitable linker.

In particular embodiments, a CAR comprises an intracellular signalingdomain. An “intracellular signaling domain,” refers to the part of a CARthat participates in transducing the message of effective CAR binding toa target antigen into the interior of the immune effector cell to eliciteffector cell function, e.g., activation, cytokine production,proliferation and cytotoxic activity, including the release of cytotoxicfactors to the CAR-bound target cell, or other cellular responseselicited with antigen binding to the extracellular CAR domain.

The term “effector function” refers to a specialized function of thecell. Effector function of the T cell, for example, may be cytolyticactivity or help or activity including the secretion of a cytokine.Thus, the term “intracellular signaling domain” refers to the portion ofa protein which transduces the effector function signal and that directsthe cell to perform a specialized function. While usually the entireintracellular signaling domain can be employed, in many cases it is notnecessary to use the entire domain. To the extent that a truncatedportion of an intracellular signaling domain is used, such truncatedportion may be used in place of the entire domain as long as ittransduces the effector function signal. The term intracellularsignaling domain is meant to include any truncated portion of theintracellular signaling domain sufficient to transducing effectorfunction signal.

It is known that signals generated through the TCR alone areinsufficient for full activation of the T cell and that a secondary orcostimulatory signal is also required. Thus, T cell activation can besaid to be mediated by two distinct classes of intracellular signalingdomains: primary signaling domains that initiate antigen-dependentprimary activation through the TCR (e.g., a TCR/CD3 complex) andcostimulatory signaling domains that act in an antigen-independentmanner to provide a secondary or costimulatory signal. In preferredembodiments, a CAR comprises an intracellular signaling domain thatcomprises one or more “costimulatory signaling domains” and a “primarysignaling domain.”

Primary signaling domains regulate primary activation of the TCR complexeither in a stimulatory way, or in an inhibitory way. Primary signalingdomains that act in a stimulatory manner may contain signaling motifswhich are known as immunoreceptor tyrosine-based activation motifs orITAMs.

Illustrative examples of ITAM containing primary signaling domainssuitable for use in CARs contemplated in particular embodiments includethose derived from FcRγ, FcRβ, CD3γ, CD3δ, CD3ε, CD3ζ, CD22, CD79a,CD79b, and CD66d. In particular preferred embodiments, a CAR comprises aCD3ζ primary signaling domain and one or more costimulatory signalingdomains. The intracellular primary signaling and costimulatory signalingdomains may be linked in any order in tandem to the carboxyl terminus ofthe transmembrane domain.

In particular embodiments, a CAR comprises one or more costimulatorysignaling domains to enhance the efficacy and expansion of T cellsexpressing CAR receptors. As used herein, the term, “costimulatorysignaling domain,” or “costimulatory domain”, refers to an intracellularsignaling domain of a costimulatory molecule.

Illustrative examples of such costimulatory molecules suitable for usein CARs contemplated in particular embodiments include TLR1, TLR2, TLR3,TLR4, TLR5, TLR6, TLR7, TLR8, TLR9, TLR10, CARD11, CD2, CD7, CD27, CD28,CD30, CD40, CD54 (ICAM), CD83, CD134 (OX40), CD137 (4-1BB), CD278(ICOS), DAP10, LAT, NKD2C, SLP76, TRIM, and ZAP70. In one embodiment, aCAR comprises one or more costimulatory signaling domains selected fromthe group consisting of CD28, CD137, and CD134, and a CD3ζ primarysignaling domain.

In various embodiments, the CAR comprises: an extracellular domain thatbinds an antigen selected from the group consisting of: BCMA, CD19,CSPG4, PSCA, ROR1, and TAG72; a transmembrane domain isolated from apolypeptide selected from the group consisting of: CD4, CD8α, CD154, andPD-1; one or more intracellular costimulatory signaling domains isolatedfrom a polypeptide selected from the group consisting of: CD28, CD134,and CD137; and a signaling domain isolated from a polypeptide selectedfrom the group consisting of: FcRγ, FcRβ, CD3γ, CD3δ, CD3ε, CD3ζ, CD22,CD79a, CD79b, and CD66d.

c. Daric Receptors

In particular embodiments, the engineered immune effector cells compriseone or more Daric receptors. As used herein, the term “Daric receptor”refers to a multi-chain engineered antigen receptor. In one embodiment,T cells comprising a polynucleotide encoding one or more Dane receptorcomponents are edited by introducing a DSB in a CBLB gene. In oneembodiment, T cells are engineered by introducing a DSB in one or moreCBLB alleles in the presence of a donor repair template encoding one ormore components of a Daric. In a particular embodiment, a Daric or oneor more components thereof is inserted at a DSB in a single CBLB allele.

In one embodiment, the engineered T cells comprise a Daric that is notinserted at a CBLB gene and one or more of an immunosuppressive signaldamper, a flip receptor, an alpha and/or beta chain of an engineered Tcell receptor (TCR), a chimeric antigen receptor (CAR), or a Daricreceptor or components thereof is inserted into a DSB in one or moreCBLB alleles.

Illustrative examples of Daric architectures and components aredisclosed in PCT Publication No. WO2015/017214 and U.S. PatentPublication No. 20150266973, each of which is incorporated here byreference in its entirety.

In one embodiment, a donor repair template comprises the following Dariccomponents: a signaling polypeptide comprising a first multimerizationdomain, a first transmembrane domain, and one or more intracellularco-stimulatory signaling domains and/or primary signaling domains; and abinding polypeptide comprising a binding domain, a secondmultimerization domain, and optionally a second transmembrane domain. Afunctional Daric comprises a bridging factor that promotes the formationof a Daric receptor complex on the cell surface with the bridging factorassociated with and disposed between the multimerization domains of thesignaling polypeptide and the binding polypeptide.

In particular embodiments, the first and second multimerization domainsassociate with a bridging factor selected from the group consisting of:rapamycin or a rapalog thereof, coumermycin or a derivative thereof,gibberellin or a derivative thereof, abscisic acid (ABA) or a derivativethereof, methotrexate or a derivative thereof, cyclosporin A or aderivative thereof, FKCsA or a derivative thereof, trimethoprim(Tmp)-synthetic ligand for FKBP (SLF) or a derivative thereof, and anycombination thereof.

Illustrative examples of rapamycin analogs (rapalogs) include thosedisclosed in U.S. Pat. No. 6,649,595, which rapalog structures areincorporated herein by reference in their entirety. In certainembodiments, a bridging factor is a rapalog with substantially reducedimmunosuppressive effect as compared to rapamycin. A “substantiallyreduced immunosuppressive effect” refers to a rapalog having at leastless than 0.1 to 0.005 times the immunosuppressive effect observed orexpected for an equimolar amount of rapamycin, as measured eitherclinically or in an appropriate in vitro (e.g., inhibition of T cellproliferation) or in vivo surrogate of human immunosuppressive activity.In one embodiment, “substantially reduced immunosuppressive effect”refers to a rapalog having an EC50 value in such an in vitro assay thatis at least 10 to 250 times larger than the EC50 value observed forrapamycin in the same assay.

Other illustrative examples of rapalogs include, but are not limited toeverolimus, novolimus, pimecrolimus, ridaforolimus, tacrolimus,temsirolimus, umirolimus, and zotarolimus.

In certain embodiments, multimerization domains will associate with abridging factor being a rapamycin or rapalog thereof. For example, thefirst and second multimerization domains are a pair selected from FKBPand FRB. FRB domains are polypeptide regions (protein “domains”) thatare capable of forming a tripartite complex with an FKBP protein andrapamycin or rapalog thereof. FRB domains are present in a number ofnaturally occurring proteins, including mTOR proteins (also referred toin the literature as FRAP, RAPT1, or RAFT) from human and other species;yeast proteins including Tor1 and Tor2; and a Candida FRAP homolog.Information concerning the nucleotide sequences, cloning, and otheraspects of these proteins is already known in the art. For example, aprotein sequence accession number for a human mTOR is GenBank AccessionNo. L34075.1 (Brown et al., Nature 369:756, 1994).

FRB domains suitable for use in particular embodiments contemplatedherein generally contain at least about 85 to about 100 amino acidresidues. In certain embodiments, an FRB amino acid sequence for use infusion proteins of this disclosure will comprise a 93 amino acidsequence Ile-2021 through Lys-2113 and a mutation of T2098L, based theamino acid sequence of GenBank Accession No. L34075.1. An FRB domain foruse in Darics contemplated in particular embodiments will be capable ofbinding to a complex of an FKBP protein bound to rapamycin or a rapalogthereof. In certain embodiments, a peptide sequence of an FRB domaincomprises (a) a naturally occurring peptide sequence spanning at leastthe indicated 93 amino acid region of human mTOR or correspondingregions of homologous proteins; (b) a variant of a naturally occurringFRB in which up to about ten amino acids, or about 1 to about 5 aminoacids or about 1 to about 3 amino acids, or in some embodiments just oneamino acid, of the naturally-occurring peptide have been deleted,inserted, or substituted; or (c) a peptide encoded by a nucleic acidmolecule capable of selectively hybridizing to a DNA molecule encoding anaturally occurring FRB domain or by a DNA sequence which would becapable, but for the degeneracy of the genetic code, of selectivelyhybridizing to a DNA molecule encoding a naturally occurring FRB domain.

FKBPs (FK506 binding proteins) are the cytosolic receptors formacrolides, such as FK506, FK520 and rapamycin, and are highly conservedacross species lines. FKBPs are proteins or protein domains that arecapable of binding to rapamycin or to a rapalog thereof and furtherforming a tripartite complex with an FRB-containing protein or fusionprotein. An FKBP domain may also be referred to as a “rapamycin bindingdomain.” Information concerning the nucleotide sequences, cloning, andother aspects of various FKBP species is known in the art (see, e.g.,Staendart et al., Nature 346:671, 1990 (human FKBP12); Kay, Biochem. J.314:361, 1996). Homologous FKBP proteins in other mammalian species, inyeast, and in other organisms are also known in the art and may be usedin the fusion proteins disclosed herein. An FKBP domain contemplated inparticular embodiments will be capable of binding to rapamycin or arapalog thereof and participating in a tripartite complex with anFRB-containing protein (as may be determined by any means, direct orindirect, for detecting such binding).

Illustrative examples of FKBP domains suitable for use in a Dariccontemplated in particular embodiments include, but are not limited to:a naturally occurring FKBP peptide sequence, preferably isolated fromthe human FKBP12 protein (GenBank Accession No. AAA58476.1) or a peptidesequence isolated therefrom, from another human FKBP, from a murine orother mammalian FKBP, or from some other animal, yeast or fungal FKBP; avariant of a naturally occurring FKBP sequence in which up to about tenamino acids, or about 1 to about 5 amino acids or about 1 to about 3amino acids, or in some embodiments just one amino acid, of thenaturally-occurring peptide have been deleted, inserted, or substituted;or a peptide sequence encoded by a nucleic acid molecule capable ofselectively hybridizing to a DNA molecule encoding a naturally occurringFKBP or by a DNA sequence which would be capable, but for the degeneracyof the genetic code, of selectively hybridizing to a DNA moleculeencoding a naturally occurring FKBP.

Other illustrative examples of multimerization domain pairs suitable foruse in a Daric contemplated in particular embodiments include, but arenot limited to include from FKBP and FRB, FKBP and calcineurin, FKBP andcyclophilin, FKBP and bacterial DHFR, calcineurin and cyclophilin, PYL1and ABI1, or GIB1 and GAI, or variants thereof.

In yet other embodiments, an anti-bridging factor blocks the associationof a signaling polypeptide and a binding polypeptide with the bridgingfactor. For example, cyclosporin or FK506 could be used as anti-bridgingfactors to titrate out rapamycin and, therefore, stop signaling sinceonly one multimerization domain is bound. In certain embodiments, ananti-bridging factor (e.g., cyclosporine, FK506) is an immunosuppressiveagent. For example, an immunosuppressive anti-bridging factor may beused to block or minimize the function of the Daric componentscontemplated in particular embodiments and at the same time inhibit orblock an unwanted or pathological inflammatory response in a clinicalsetting.

In one embodiment, the first multimerization domain comprises FRBT2098L, the second multimerization domain comprises FKBP12, and thebridging factor is rapalog AP21967.

In another embodiment, the first multimerization domain comprises FRB,the second multimerization domain comprises FKBP12, and the bridgingfactor is Rapamycin, temsirolimus or everolimus.

In particular embodiments, a signaling polypeptide a first transmembranedomain and a binding polypeptide comprises a second transmembrane domainor GPI anchor. Illustrative examples of the first and secondtransmembrane domains are isolated from a polypeptide independentlyselected from the group consisting of: CD3δ, CD3ε, CD3γ, CD3ζ, CD4, CD5,CD8α, CD9, CD 16, CD22, CD27, CD28, CD33, CD37, CD45, CD64, CD80, CD86,CD 134, CD137, CD152, CD154, AMN, and PD-1.

In one embodiment, a signaling polypeptide comprises one or moreintracellular co-stimulatory signaling domains and/or primary signalingdomains.

Illustrative examples of primary signaling domains suitable for use inDaric signaling components contemplated in particular embodimentsinclude those derived from FcRγ, FcRβ, CD3γ, CD3δ, CD3ε, CD3ζ, CD22,CD79a, CD79b, and CD66d. In particular preferred embodiments, a Daricsignaling component comprises a CD3ζ primary signaling domain and one ormore costimulatory signaling domains. The intracellular primarysignaling and costimulatory signaling domains may be linked in any orderin tandem to the carboxyl terminus of the transmembrane domain.

Illustrative examples of such costimulatory molecules suitable for usein Daric signaling components contemplated in particular embodimentsinclude TLR1, TLR2, TLR3, TLR4, TLR5, TLR6, TLR7, TLR8, TLR9, TLR10,CARD11, CD2, CD7, CD27, CD28, CD30, CD40, CD54 (ICAM), CD83, CD134(OX40), CD137 (4-1BB), CD278 (ICOS), DAP10, LAT, NKD2C, SLP76, TRIM, andZAP70. In one embodiment, a Daric signaling component comprises one ormore costimulatory signaling domains selected from the group consistingof CD28, CD137, and CD134, and a CD3ζ primary signaling domain.

In particular embodiments, a Daric binding component comprises a bindingdomain. In one embodiment, the binding domain is an antibody or antigenbinding fragment thereof.

The antibody or antigen binding fragment thereof comprises at least alight chain or heavy chain immunoglobulin variable region whichspecifically recognizes and binds an epitope of a target antigen, suchas a peptide, lipid, polysaccharide, or nucleic acid containing anantigenic determinant, such as those recognized by an immune cell.Antibodies include antigen binding fragments, e.g., Camel Ig (a camelidantibody or VHH fragment thereof), Ig NAR, Fab fragments, Fab′fragments, F(ab)′2 fragments, F(ab)′3 fragments, Fv, single chain Fvantibody (“scFv”), bis-scFv, (scFv)2, minibody, diabody, triabody,tetrabody, disulfide stabilized Fv protein (“dsFv”), and single-domainantibody (sdAb, Nanobody) or other antibody fragments thereof. The termalso includes genetically engineered forms such as chimeric antibodies(for example, humanized murine antibodies), heteroconjugate antibodies(such as, bispecific antibodies) and antigen binding fragments thereof.See also, Pierce Catalog and Handbook, 1994-1995 (Pierce Chemical Co.,Rockford, Ill.); Kuby, J., Immunology, 3rd Ed., W. H. Freeman & Co., NewYork, 1997.

In one preferred embodiment, the binding domain is an scFv.

In another preferred embodiment, the binding domain is a camelidantibody.

In particular embodiments, the Daric binding component comprises anextracellular domain that binds an antigen selected from the groupconsisting of: alpha folate receptor, 5T4, αvβ6 integrin, BCMA, B7-H3,B7-H6, CAIX, CD16, CD19, CD20, CD22, CD30, CD33, CD44, CD44v6, CD44v7/8,CD70, CD79a, CD79b, CD123, CD138, CD171, CEA, CSPG4, EGFR, EGFR familyincluding ErbB2 (HER2), EGFRvIII, EGP2, EGP40, EPCAM, EphA2, EpCAM, FAP,fetal AchR, GD2, GD3, Glypican-3 (GPC3), HLA-A1+MAGE1, HLA-A2+MAGE1,HLA-A3+MAGE1, HLA-A1+NY-ESO-1, HLA-A2+NY-ESO-1, HLA-A3+NY-ESO-1,IL-11Rα, IL-13Rα2, Lambda, Lewis-Y, Kappa, Mesothelin, Muc1, Muc16,NCAM, NKG2D Ligands, NY-ESO-1, PRAME, PSCA, PSMA, ROR1, SSX, Survivin,TAG72, TEMs, VEGFR2, and WT-1.

In one embodiment, the Daric binding component comprises anextracellular domain, e.g., antibody or antigen binding fragment thereofthat binds an MHC-peptide complex, such as a class I MHC-peptide complexor class II MHC-peptide complex.

In particular embodiments, the Daric components contemplated hereincomprise a linker or spacer that connects two proteins, polypeptides,peptides, domains, regions, or motifs. In certain embodiments, a linkercomprises about two to about 35 amino acids, or about four to about 20amino acids or about eight to about 15 amino acids or about 15 to about25 amino acids. In other embodiments, a spacer may have a particularstructure, such as an antibody CH2CH3 domain, hinge domain or the like.In one embodiment, a spacer comprises the CH2 and CH3 domains of IgG1,IgG4, or IgD.

In particular embodiments, the Daric components contemplated hereincomprise one or more “hinge domains,” which plays a role in positioningthe domains to enable proper cell/cell contact, antigen binding andactivation. A Daric may comprise one or more hinge domains between thebinding domain and the multimerization domain and/or the transmembranedomain (TM) or between the multimerization domain and the transmembranedomain. The hinge domain may be derived either from a natural,synthetic, semi-synthetic, or recombinant source. The hinge domain caninclude the amino acid sequence of a naturally occurring immunoglobulinhinge region or an altered immunoglobulin hinge region. In particularembodiment, the hinge is a CD8α hinge or a CD4 hinge.

In one embodiment, a Daric comprises a signaling polypeptide comprises afirst multimerization domain of FRB T2098L, a CD8 transmembrane domain,a 4-1BB costimulatory domain, and a CD3ζ primary signaling domain; thebinding polypeptide comprises an scFv that binds CD19, a secondmultimerization domain of FKBP12 and a CD4 transmembrane domain; and thebridging factor is rapalog AP21967.

In one embodiment, a Daric comprises a signaling polypeptide comprises afirst multimerization domain of FRB, a CD8 transmembrane domain, a 4-1BBcostimulatory domain, and a CD3ζ primary signaling domain; the bindingpolypeptide comprises an scFv that binds CD19, a second multimerizationdomain of FKBP12 and a CD4 transmembrane domain; and the bridging factoris Rapamycin, temsirolimus or everolimus.

d. Zetakines

In particular embodiments, the engineered immune effector cellscontemplated herein comprise one or more chimeric cytokine receptors. Inone embodiment, T cells comprising a polynucleotide encoding a zetakineare edited by introducing a DSB in a CBLB gene. In one embodiment, Tcells are engineered by introducing a DSB in one or more CBLB alleles inthe presence of a donor repair template encoding a CAR. In a particularembodiment, a chimeric cytokine receptor is inserted at a DSB in asingle CBLB allele.

In one embodiment, the engineered T cells contemplated herein a chimericcytokine receptor that is not inserted at a CBLB gene and one or more ofan immunosuppressive signal damper, a flip receptor, an alpha and/orbeta chain of an engineered T cell receptor (TCR), a chimeric antigenreceptor (CAR), a Daric receptor or components thereof, or a chimericcytokine receptor is inserted into a DSB in one or more CBLB alleles.

In various embodiments, the genome edited T cells express chimericcytokine receptor that redirect cytotoxicity toward tumor cells.Zetakines are chimeric transmembrane immunoreceptors that comprise anextracellular domain comprising a soluble receptor ligand linked to asupport region capable of tethering the extracellular domain to a cellsurface, a transmembrane region and an intracellular signaling domain.Zetakines, when expressed on the surface of T lymphocytes, direct T cellactivity to those cells expressing a receptor for which the solublereceptor ligand is specific. Zetakine chimeric immunoreceptors redirectthe antigen specificity of T cells, with application to treatment of avariety of cancers, particularly via the autocrine/paracrine cytokinesystems utilized by human malignancy.

In particular embodiments, the chimeric cytokine receptor comprises animmunosuppressive cytokine or cytokine receptor binding variant thereof,a linker, a transmembrane domain, and an intracellular signaling domain.

In particular embodiments, the cytokine or cytokine receptor bindingvariant thereof is selected from the group consisting of: interleukin-4(IL-4), interleukin-6 (IL-6), interleukin-8 (IL-8), interleukin-10(IL-10), and interleukin-13 (IL-13).

In certain embodiments, the linker comprises a CH2CH3 domain, hingedomain, or the like. In one embodiment, a linker comprises the CH2 andCH3 domains of IgG1, IgG4, or IgD. In one embodiment, a linker comprisesa CD8α or CD4 hinge domain.

In particular embodiments, the transmembrane domain is selected from thegroup consisting of: the alpha or beta chain of the T-cell receptor,CD3δ, CD3ε, CD3γ, CD3ζ, CD4, CDS, CD8α, CD9, CD 16, CD22, CD27, CD28,CD33, CD37, CD45, CD64, CD80, CD86, CD 134, CD137, CD152, CD154, AMN,and PD-1.

In particular embodiments, the intracellular signaling domain isselected from the group consisting of: an ITAM containing primarysignaling domain and/or a costimulatory domain.

In particular embodiments, the intracellular signaling domain isselected from the group consisting of: FcRγ, FcRβ, CD3γ, CD3δ, CD3ε,CD3ζ, CD22, CD79a, CD79b, and CD66d.

In particular embodiments, the intracellular signaling domain isselected from the group consisting of: TLR1, TLR2, TLR3, TLR4, TLR5,TLR6, TLR7, TLR8, TLR9, TLR10, CARD11, CD2, CD7, CD27, CD28, CD30, CD40,CD54 (ICAM), CD83, CD134 (OX40), CD137 (4-1BB), CD278 (ICOS), DAP10,LAT, NKD2C, SLP76, TRIM, and ZAP70.

In one embodiment, a chimeric cytokine receptor comprises one or morecostimulatory signaling domains selected from the group consisting ofCD28, CD137, and CD134, and a CD3ζ primary signaling domain.

F. Polypeptides

Various polypeptides are contemplated herein, including, but not limitedto, homing endonuclease variants, megaTALs, and fusion polypeptides. Inpreferred embodiments, a polypeptide comprises the amino acid sequenceset forth in SEQ ID NOs: 1-19 and 38. “Polypeptide,” “polypeptidefragment,” “peptide” and “protein” are used interchangeably, unlessspecified to the contrary, and according to conventional meaning, i.e.,as a sequence of amino acids. In one embodiment, a “polypeptide”includes fusion polypeptides and other variants. Polypeptides can beprepared using any of a variety of well-known recombinant and/orsynthetic techniques. Polypeptides are not limited to a specific length,e.g., they may comprise a full-length protein sequence, a fragment of afull-length protein, or a fusion protein, and may includepost-translational modifications of the polypeptide, for example,glycosylations, acetylations, phosphorylations and the like, as well asother modifications known in the art, both naturally occurring andnon-naturally occurring.

An “isolated protein,” “isolated peptide,” or “isolated polypeptide” andthe like, as used herein, refer to in vitro synthesis, isolation, and/orpurification of a peptide or polypeptide molecule from a cellularenvironment, and from association with other components of the cell,i.e., it is not significantly associated with in vivo substances.

Illustrative examples of polypeptides contemplated in particularembodiments include, but are not limited to homing endonucleasevariants, megaTALs, BiTEs, cytokines, chemokines, cytotoxins, andcytokine receptors, flip receptors, immunosuppressive signal dampers,CARs, DARICs, TCRs, and zetakines.

Polypeptides include “polypeptide variants.” Polypeptide variants maydiffer from a naturally occurring polypeptide in one or more amino acidsubstitutions, deletions, additions and/or insertions. Such variants maybe naturally occurring or may be synthetically generated, for example,by modifying one or more amino acids of the above polypeptide sequences.For example, in particular embodiments, it may be desirable to improvethe biological properties of a homing endonuclease, megaTAL or the likethat binds and cleaves a target site in the human CBLB gene byintroducing one or more substitutions, deletions, additions and/orinsertions into the polypeptide. In particular embodiments, polypeptidesinclude polypeptides having at least about 65%, 70%, 71%, 72%, 73%, 74%,75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%,85%, 86%, 87%, 88%,89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% amino acididentity to any of the reference sequences contemplated herein,typically where the variant maintains at least one biological activityof the reference sequence.

Polypeptide variants include biologically active “polypeptidefragments.” Illustrative examples of biologically active polypeptidefragments include DNA binding domains, nuclease domains, and the like.As used herein, the term “biologically active fragment” or “minimalbiologically active fragment” refers to a polypeptide fragment thatretains at least 100%, at least 90%, at least 80%, at least 70%, atleast 60%, at least 50%, at least 40%, at least 30%, at least 20%, atleast 10%, or at least 5% of the naturally occurring polypeptideactivity. In preferred embodiments, the biological activity is bindingaffinity and/or cleavage activity for a target sequence. In certainembodiments, a polypeptide fragment can comprise an amino acid chain atleast 5 to about 1700 amino acids long. It will be appreciated that incertain embodiments, fragments are at least 5, 6, 7, 8, 9, 10, 11, 12,13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30,31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48,49, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 110, 150, 200, 250,300, 350, 400, 450, 500, 550, 600, 650, 700, 750, 800, 850, 900, 950,1000, 1100, 1200, 1300, 1400, 1500, 1600, 1700 or more amino acids long.In particular embodiments, a polypeptide comprises a biologically activefragment of a homing endonuclease variant. In particular embodiments,the polypeptides set forth herein may comprise one or more amino acidsdenoted as “X.” “X” if present in an amino acid SEQ ID NO, refers to anyamino acid. One or more “X” residues may be present at the N- andC-terminus of an amino acid sequence set forth in particular SEQ ID NOscontemplated herein. If the “X” amino acids are not present theremaining amino acid sequence set forth in a SEQ ID NO may be considereda biologically active fragment.

In particular embodiments, a polypeptide comprises a biologically activefragment of a homing endonuclease variant, e.g., SEQ ID NOs: 3-12, or amegaTAL (SEQ ID NOs: 13-19). The biologically active fragment maycomprise an N-terminal truncation and/or C-terminal truncation. In aparticular embodiment, a biologically active fragment lacks or comprisesa deletion of the 1, 2, 3, 4, 5, 6, 7, or 8 N-terminal amino acids of ahoming endonuclease variant compared to a corresponding wild type homingendonuclease sequence, more preferably a deletion of the 4 N-terminalamino acids of a homing endonuclease variant compared to a correspondingwild type homing endonuclease sequence. In a particular embodiment, abiologically active fragment lacks or comprises a deletion of the 1, 2,3, 4, or 5 C-terminal amino acids of a homing endonuclease variantcompared to a corresponding wild type homing endonuclease sequence, morepreferably a deletion of the 2 C-terminal amino acids of a homingendonuclease variant compared to a corresponding wild type homingendonuclease sequence. In a particular preferred embodiment, abiologically active fragment lacks or comprises a deletion of the 4N-terminal amino acids and 2 C-terminal amino acids of a homingendonuclease variant compared to a corresponding wild type homingendonuclease sequence.

In a particular embodiment, an I-OnuI variant comprises a deletion of 1,2, 3, 4, 5, 6, 7, or 8 the following N-terminal amino acids: M, A, Y, M,S, R, R, E; and/or a deletion of the following 1, 2, 3, 4, or 5C-terminal amino acids: R, G, S, F, V.

In a particular embodiment, an I-OnuI variant comprises a deletion orsubstitution of 1, 2, 3, 4, 5, 6, 7, or 8 the following N-terminal aminoacids: M, A, Y, M, S, R, R, E; and/or a deletion or substitution of thefollowing 1, 2, 3, 4, or 5 C-terminal amino acids: R, G, S, F, V.

As noted above, polypeptides may be altered in various ways includingamino acid substitutions, deletions, truncations, and insertions.Methods for such manipulations are generally known in the art. Forexample, amino acid sequence variants of a reference polypeptide can beprepared by mutations in the DNA. Methods for mutagenesis and nucleotidesequence alterations are well known in the art. See, for example, Kunkel(1985, Proc. Natl. Acari Sci. USA. 82: 488-492), Kunkel et al., (1987,Methods in Enzymol, 154: 367-382), U.S. Pat. No. 4,873,192, Watson, J.D. et al., (Molecular Biology of the Gene, Fourth Edition,Benjamin/Cummings, Menlo Park, Calif., 1987) and the references citedtherein. Guidance as to appropriate amino acid substitutions that do notaffect biological activity of the protein of interest may be found inthe model of Dayhoff et al., (1978) Atlas of Protein Sequence andStructure (Natl. Biomed. Res. Found, Washington, D.C.).

In certain embodiments, a variant will contain one or more conservativesubstitutions. A “conservative substitution” is one in which an aminoacid is substituted for another amino acid that has similar properties,such that one skilled in the art of peptide chemistry would expect thesecondary structure and hydropathic nature of the polypeptide to besubstantially unchanged. Modifications may be made in the structure ofthe polynucleotides and polypeptides contemplated in particularembodiments, polypeptides include polypeptides having at least about andstill obtain a functional molecule that encodes a variant or derivativepolypeptide with desirable characteristics. When it is desired to alterthe amino acid sequence of a polypeptide to create an equivalent, oreven an improved, variant polypeptide, one skilled in the art, forexample, can change one or more of the codons of the encoding DNAsequence, e.g., according to Table 1.

TABLE 1 Amino Acid Codons One Three Amino  letter letter Acids code codeCodons Alanine A Ala GCA GCC GCG GCU Cysteine C Cys UGC UGU Aspartic  DAsp GAC GAU acid Glutamic E Glu GAA GAG acid Phenylalanine F Phc UUC UUUGlycine G Gly GGA GGC GGG GGU Histidine H His CAC CAU Isoleucine 1 IsoAUA AUC AUU Lysine K Lys AAA AAG Leucine L Leu UUA UUG CUA CUC CUG CUUMethionine M Met AUG Asparagine N Asn AAC AAU Proline P Pro CCA CCC CCGCCU Glutamine Q Gln CAA CAG Arginine R Arg AGA AGG CGA CGC CGG CGUSerine S Ser AGC AGU UCA UCC UCG UCU Threonine T Thr ACA ACC ACG ACUValine V Val GUA GUC GUG GUU Tryptophan W Trp UGG Tyrosine Y Tyr UAC UAU

Guidance in determining which amino acid residues can be substituted,inserted, or deleted without abolishing biological activity can be foundusing computer programs well known in the art, such as DNASTAR, GCG, DNAStrider, Geneious, Mac Vector, or Vector NTI software. Preferably, aminoacid changes in the protein variants disclosed herein are conservativeamino acid changes, i.e., substitutions of similarly charged oruncharged amino acids. A conservative amino acid change involvessubstitution of one of a family of amino acids which are related intheir side chains. Naturally occurring amino acids are generally dividedinto four families: acidic (aspartate, glutamate), basic (lysine,arginine, histidine), non-polar (alanine, valine, leucine, isoleucine,proline, phenylalanine, methionine, tryptophan), and uncharged polar(glycine, asparagine, glutamine, cysteine, serine, threonine, tyrosine)amino acids. Phenylalanine, tryptophan, and tyrosine are sometimesclassified jointly as aromatic amino acids. In a peptide or protein,suitable conservative substitutions of amino acids are known to those ofskill in this art and generally can be made without altering abiological activity of a resulting molecule. Those of skill in this artrecognize that, in general, single amino acid substitutions innon-essential regions of a polypeptide do not substantially alterbiological activity (see, e.g., Watson et al. Molecular Biology of theGene, 4th Edition, 1987, The Benjamin/Cummings Pub. Co., p. 224).

In one embodiment, where expression of two or more polypeptides isdesired, the polynucleotide sequences encoding them can be separated byand IRES sequence as disclosed elsewhere herein.

Polypeptides contemplated in particular embodiments include fusionpolypeptides. In particular embodiments, fusion polypeptides andpolynucleotides encoding fusion polypeptides are provided. Fusionpolypeptides and fusion proteins refer to a polypeptide having at leasttwo, three, four, five, six, seven, eight, nine, or ten polypeptidesegments.

In another embodiment, two or more polypeptides can be expressed as afusion protein that comprises one or more self-cleaving polypeptidesequences as disclosed elsewhere herein.

In one embodiment, a fusion protein contemplated herein comprises one ormore DNA binding domains and one or more nucleases, and one or morelinker and/or self-cleaving polypeptides.

In one embodiment, a fusion protein contemplated herein comprisesnuclease variant; a linker or self-cleaving peptide; and anend-processing enzyme including but not limited to a 5′-3′ exonuclease,a 5′-3′ alkaline exonuclease, and a 3′-5′ exonuclease (e.g., Trex2).

Fusion polypeptides can comprise one or more polypeptide domains orsegments including, but are not limited to signal peptides, cellpermeable peptide domains (CPP), DNA binding domains, nuclease domains,etc., epitope tags (e.g., maltose binding protein (“MBP”), glutathione Stransferase (GST), HIS6, MYC, FLAG, V5, VSV-G, and HA), polypeptidelinkers, and polypeptide cleavage signals. Fusion polypeptides aretypically linked C-terminus to N-terminus, although they can also belinked C-terminus to C-terminus, N-terminus to N-terminus, or N-terminusto C-terminus. In particular embodiments, the polypeptides of the fusionprotein can be in any order. Fusion polypeptides or fusion proteins canalso include conservatively modified variants, polymorphic variants,alleles, mutants, subsequences, and interspecies homologs, so long asthe desired activity of the fusion polypeptide is preserved. Fusionpolypeptides may be produced by chemical synthetic methods or bychemical linkage between the two moieties or may generally be preparedusing other standard techniques. Ligated DNA sequences comprising thefusion polypeptide are operably linked to suitable transcriptional ortranslational control elements as disclosed elsewhere herein.

Fusion polypeptides may optionally comprise a linker that can be used tolink the one or more polypeptides or domains within a polypeptide. Apeptide linker sequence may be employed to separate any two or morepolypeptide components by a distance sufficient to ensure that eachpolypeptide folds into its appropriate secondary and tertiary structuresso as to allow the polypeptide domains to exert their desired functions.Such a peptide linker sequence is incorporated into the fusionpolypeptide using standard techniques in the art. Suitable peptidelinker sequences may be chosen based on the following factors: (1) theirability to adopt a flexible extended conformation; (2) their inabilityto adopt a secondary structure that could interact with functionalepitopes on the first and second polypeptides; and (3) the lack ofhydrophobic or charged residues that might react with the polypeptidefunctional epitopes. Preferred peptide linker sequences contain Gly, Asnand Ser residues. Other near neutral amino acids, such as Thr and Alamay also be used in the linker sequence. Amino acid sequences which maybe usefully employed as linkers include those disclosed in Maratea etal., Gene 40:39-46, 1985; Murphy et al., Proc. Natl. Acad. Sci. USA83:8258-8262, 1986; U.S. Pat. Nos. 4,935,233 and 4,751,180. Linkersequences are not required when a particular fusion polypeptide segmentcontains non-essential N-terminal amino acid regions that can be used toseparate the functional domains and prevent steric interference.Preferred linkers are typically flexible amino acid subsequences whichare synthesized as part of a recombinant fusion protein. Linkerpolypeptides can be between 1 and 200 amino acids in length, between 1and 100 amino acids in length, or between 1 and 50 amino acids inlength, including all integer values in between.

Exemplary linkers include, but are not limited to the following aminoacid sequences: glycine polymers (G)_(n); glycine-serine polymers(G₁₋₅S₁₋₅)_(n), where n is an integer of at least one, two, three, four,or five; glycine-alanine polymers; alanine-serine polymers; GGG (SEQ IDNO: 39); DGGGS (SEQ ID NO: 40); TGEKP (SEQ ID NO: 41) (see e.g., Liu etal., PNAS 5525-5530 (1997)); GGRR (SEQ ID NO: 42) (Pomerantz et al.1995, supra); (GGGGS)_(n) wherein n=1, 2, 3, 4 or 5 (SEQ ID NO: 43) (Kimet al., PNAS 93, 1156-1160 (1996.); EGKSSGSGSESKVD (SEQ ID NO: 44)(Chaudhary et al., 1990, Proc. Natl. Acad. Sci. U.S.A. 87:1066-1070);KESGSVSSEQLAQFRSLD (SEQ ID NO: 45) (Bird et al., 1988, Science242:423-426), GGRRGGGS (SEQ ID NO: 46); LRQRDGERP (SEQ ID NO: 47);LRQKDGGGSERP (SEQ ID NO: 48); LRQKD(GGGS)₂ERP (SEQ ID NO: 49).Alternatively, flexible linkers can be rationally designed using acomputer program capable of modeling both DNA-binding sites and thepeptides themselves (Desjarlais & Berg, PNAS 90:2256-2260 (1993), PNAS91:11099-11103 (1994) or by phage display methods.

Fusion polypeptides may further comprise a polypeptide cleavage signalbetween each of the polypeptide domains described herein or between anendogenous open reading frame and a polypeptide encoded by a donorrepair template. In addition, a polypeptide cleavage site can be putinto any linker peptide sequence. Exemplary polypeptide cleavage signalsinclude polypeptide cleavage recognition sites such as protease cleavagesites, nuclease cleavage sites (e.g., rare restriction enzymerecognition sites, self-cleaving ribozyme recognition sites), andself-cleaving viral oligopeptides (see deFelipe and Ryan, 2004. Traffic,5(8); 616-26).

Suitable protease cleavages sites and self-cleaving peptides are knownto the skilled person (see, e.g., in Ryan et al., 1997. J. Gener. Virol.78, 699-722; Scymczak et al. (2004) Nature Biotech. 5, 589-594).Exemplary protease cleavage sites include, but are not limited to thecleavage sites of potyvirus NIa proteases (e.g., tobacco etch virusprotease), potyvirus HC proteases, potyvirus P1 (P35) proteases,byovirus NIa proteases, byovirus RNA-2-encoded proteases, aphthovirus Lproteases, enterovirus 2A proteases, rhinovirus 2A proteases, picorna 3Cproteases, comovirus 24K proteases, nepovirus 24K proteases, RTSV (ricetungro spherical virus) 3C-like protease, PYVF (parsnip yellow fleckvirus) 3C-like protease, heparin, thrombin, factor Xa and enterokinase.Due to its high cleavage stringency, TEV (tobacco etch virus) proteasecleavage sites are preferred in one embodiment, e.g., EXXYXQ(G/S) (SEQID NO: 50), for example, ENLYFQG (SEQ ID NO: 51) and ENLYFQS (SEQ ID NO:52), wherein X represents any amino acid (cleavage by TEV occurs betweenQ and G or Q and S).

In certain embodiments, the self-cleaving polypeptide site comprises a2A or 2A-like site, sequence or domain (Donnelly et al., 2001. J. Gen.Virol. 82:1027-1041). In a particular embodiment, the viral 2A peptideis an aphthovirus 2A peptide, a potyvirus 2A peptide, or a cardiovirus2A peptide.

In one embodiment, the viral 2A peptide is selected from the groupconsisting of: a foot-and-mouth disease virus (FMDV) (F2A) peptide, anequine rhinitis A virus (ERAV) (E2A) peptide, a Thosea asigna virus(TaV) (T2A) peptide, a porcine teschovirus-1 (PTV-1) (P2A) peptide, aTheilovirus 2A peptide, and an encephalomyocarditis virus 2A peptide.

Illustrative examples of 2A sites are provided in Table 2.

TABLE 2 Exemplary 2A sites include the following sequences:SEQ ID NO: 53 GSGATNFSLLKQAGDVEENPGP SEQ ID NO: 54 ATNFSLLKQAGDVEENPGPSEQ ID NO: 55 LLKQAGDVEENPGP SEQ ID NO: 56 GSGEGRGSLLTCGDVEENPGPSEQ ID NO: 57 EGRGSLLTCGDVEENPGP SEQ ID NO: 58 LLTCGDVEENPGPSEQ ID NO: 59 GSGQCTNYALLKLAGDVESNPGP SEQ ID NO: 60 QCTNYALLKLAGDVESNPGPSEQ ID NO: 61 LLKLAGDVESNPGP SEQ ID NO: 62 GSGVKQTLNFDLLKLAGDVESNPGPSEQ ID NO: 63 VKQTLNFDLLKLAGDVESNPGP SEQ ID NO: 64 LLKLAGDVESNPGPSEQ ID NO: 65 LLNFDLLKLAGDVESNPGP SEQ ID NO: 66 TLNFDLLKLAGDVESNPGPSEQ ID NO: 67 LLKLAGDVESNPGP SEQ ID NO: 68 NFDLLKLAGDVESNPGPSEQ ID NO: 69 QLLNFDLLKLAGDVESNPGP SEQ ID NO: 70APVKQTLNFDLLKLAGDVESNPGP SEQ ID NO: 71  VTELLYRMKRAETYCPRPLLAIHPIEARHKQKIVAPVKQT SEQ ID NO: 72 LNFDLLKLAGDVESNPGP SEQ ID NO: 73LLAIHPTEARHKQKIVAPVKQ TLNFDLLKLAGDVESNPGP SEQ ID NO: 74EARHKQKIVAPVKQTLNFDLL KLAGDVESNPGP

G. Polynucleotides

In particular embodiments, polynucleotides encoding one or more homingendonuclease variants, megaTALs, end-processing enzymes, and fusionpolypeptides or one or more biologically active fragments or variantscontemplated herein are provided. As used herein, the terms“polynucleotide” or “nucleic acid” refer to deoxyribonucleic acid (DNA),ribonucleic acid (RNA) and DNA/RNA hybrids. Polynucleotides may besingle-stranded or double-stranded and either recombinant, synthetic, orisolated. Polynucleotides include, but are not limited to: pre-messengerRNA (pre-mRNA), messenger RNA (mRNA), RNA, short interfering RNA(siRNA), short hairpin RNA (shRNA), microRNA (miRNA), ribozymes, genomicRNA (gRNA), plus strand RNA (RNA(+)), minus strand RNA (RNA(−)),tracrRNA, crRNA, single guide RNA (sgRNA), synthetic RNA, syntheticmRNA, genomic DNA (gDNA), PCR amplified DNA, complementary DNA (cDNA),synthetic DNA, or recombinant DNA. In particular embodiments, apolynucleotides is a polynucleotide fragments that encodes one or morebiologically active polypeptide fragments or variants. Polynucleotidesrefer to a polymeric form of nucleotides of at least 5, at least 10, atleast 15, at least 20, at least 25, at least 30, at least 40, at least50, at least 100, at least 200, at least 300, at least 400, at least500, at least 1000, at least 5000, at least 10000, or at least 15000 ormore nucleotides in length, either ribonucleotides ordeoxyribonucleotides or a modified form of either type of nucleotide, aswell as all intermediate lengths. It will be readily understood that“intermediate lengths, ” in this context, means any length between thequoted values, such as 6, 7, 8, 9, etc., 101, 102, 103, etc.; 151, 152,153, etc.; 201, 202, 203, etc. In particular embodiments,polynucleotides or variants have at least or about 50%, 55%, 60%, 65%,70%, 71%, 72%, 73%, 74%, 75%,76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%,84%,85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%,98%, 99% or 100% sequence identity to a reference sequence.

In particular embodiments, polynucleotides may be codon-optimized. Asused herein, the term “codon-optimized” refers to substituting codons ina polynucleotide encoding a polypeptide in order to increase theexpression, stability and/or activity of the polypeptide. Factors thatinfluence codon optimization include, but are not limited to one or moreof: (i) variation of codon biases between two or more organisms or genesor synthetically constructed bias tables, (ii) variation in the degreeof codon bias within an organism, gene, or set of genes, (iii)systematic variation of codons including context, (iv) variation ofcodons according to their decoding tRNAs, (v) variation of codonsaccording to GC %, either overall or in one position of the triplet,(vi) variation in degree of similarity to a reference sequence forexample a naturally occurring sequence, (vii) variation in the codonfrequency cutoff, (viii) structural properties of mRNAs transcribed fromthe DNA sequence, (ix) prior knowledge about the function of the DNAsequences upon which design of the codon substitution set is to bebased, (x) systematic variation of codon sets for each amino acid,and/or (xi) isolated removal of spurious translation initiation sites.

As used herein the term “nucleotide” refers to a heterocyclicnitrogenous base in N-glycosidic linkage with a phosphorylated sugar.Nucleotides are understood to include natural bases, and a wide varietyof art-recognized modified bases. Such bases are generally located atthe position of a nucleotide sugar moiety. Nucleotides generallycomprise a base, sugar and a phosphate group. In ribonucleic acid (RNA),the sugar is a ribose, and in deoxyribonucleic acid (DNA) the sugar is adeoxyribose, i.e., a sugar lacking a hydroxyl group that is present inribose. Exemplary natural nitrogenous bases include the purines,adenosine (A) and guanidine (G), and the pyrimidines, cytidine (C) andthymidine (T) (or in the context of RNA, uracil (U)). The C-1 atom ofdeoxyribose is bonded to N-1 of a pyrimidine or N-9 of a purine.Nucleotides are usually mono, di- or triphosphates. The nucleotides canbe unmodified or modified at the sugar, phosphate and/or base moiety,(also referred to interchangeably as nucleotide analogs, nucleotidederivatives, modified nucleotides, non-natural nucleotides, andnon-standard nucleotides; see for example, WO 92/07065 and WO 93/15187).Examples of modified nucleic acid bases are summarized by Limbach etal., (1994, Nucleic Acids Res. 22, 2183-2196).

A nucleotide may also be regarded as a phosphate ester of a nucleoside,with esterification occurring on the hydroxyl group attached to C-5 ofthe sugar. As used herein, the term “nucleoside” refers to aheterocyclic nitrogenous base in N-glycosidic linkage with a sugar.Nucleosides are recognized in the art to include natural bases, and alsoto include well known modified bases. Such bases are generally locatedat the position of a nucleoside sugar moiety. Nucleosides generallycomprise a base and sugar group. The nucleosides can be unmodified ormodified at the sugar, and/or base moiety, (also referred tointerchangeably as nucleoside analogs, nucleoside derivatives, modifiednucleosides, non-natural nucleosides, or non-standard nucleosides). Asalso noted above, examples of modified nucleic acid bases are summarizedby Limbach et al., (1994, Nucleic Acids Res. 22, 2183-2196).

Illustrative examples of polynucleotides include, but are not limited topolynucleotides encoding SEQ ID NOs: 1-19 and 38, and polynucleotidesequences set forth in SEQ ID NOs: 20-37.

In various illustrative embodiments, polynucleotides contemplated hereininclude, but are not limited to polynucleotides encoding homingendonuclease variants, megaTALs, end-processing enzymes, fusionpolypeptides, and expression vectors, viral vectors, and transferplasmids comprising polynucleotides contemplated herein.

As used herein, the terms “polynucleotide variant” and “variant” and thelike refer to polynucleotides displaying substantial sequence identitywith a reference polynucleotide sequence or polynucleotides thathybridize with a reference sequence under stringent conditions that aredefined hereinafter. These terms also encompass polynucleotides that aredistinguished from a reference polynucleotide by the addition, deletion,substitution, or modification of at least one nucleotide. Accordingly,the terms “polynucleotide variant” and “variant” include polynucleotidesin which one or more nucleotides have been added or deleted, ormodified, or replaced with different nucleotides. In this regard, it iswell understood in the art that certain alterations inclusive ofmutations, additions, deletions and substitutions can be made to areference polynucleotide whereby the altered polynucleotide retains thebiological function or activity of the reference polynucleotide.

Polynucleotide variants include polynucleotide fragments that encodebiologically active polypeptide fragments or variants. As used herein,the term “polynucleotide fragment” refers to a polynucleotide fragmentat least 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21,22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39,40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 55, 60, 65, 70, 75, 80, 85,90, 95, 100, 110, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600, 650,700, 750, 800, 850, 900, 950, 1000, 1100, 1200, 1300, 1400, 1500, 1600,1700 or more nucleotides in length that encodes a polypeptide variantthat retains at least 100%, at least 90%, at least 80%, at least 70%, atleast 60%, at least 50%, at least 40%, at least 30%, at least 20%, atleast 10%, or at least 5% of the naturally occurring polypeptideactivity. Polynucleotide fragments refer to a polynucleotide thatencodes a polypeptide that has an amino-terminal deletion, acarboxyl-terminal deletion, and/or an internal deletion or substitutionof one or more amino acids of a naturally-occurring orrecombinantly-produced polypeptide.

In one embodiment, a polynucleotide comprises a nucleotide sequence thathybridizes to a target nucleic acid sequence under stringent conditions.To hybridize under “stringent conditions” describes hybridizationprotocols in which nucleotide sequences at least 60% identical to eachother remain hybridized. Generally, stringent conditions are selected tobe about 5° C. lower than the thermal melting point (Tm) for thespecific sequence at a defined ionic strength and pH. The Tm is thetemperature (under defined ionic strength, pH and nucleic acidconcentration) at which 50% of the probes complementary to the targetsequence hybridize to the target sequence at equilibrium. Since thetarget sequences are generally present at excess, at Tm, 50% of theprobes are occupied at equilibrium.

The recitations “sequence identity” or, for example, comprising a“sequence 50% identical to,” as used herein, refer to the extent thatsequences are identical on a nucleotide-by-nucleotide basis or an aminoacid-by-amino acid basis over a window of comparison. Thus, a“percentage of sequence identity” may be calculated by comparing twooptimally aligned sequences over the window of comparison, determiningthe number of positions at which the identical nucleic acid base (e.g.,A, T, C, G, I) or the identical amino acid residue (e.g., Ala, Pro, Ser,Thr, Gly, Val, Leu, Ile, Phe, Tyr, Trp, Lys, Arg, His, Asp, Glu, Asn,Gln, Cys and Met) occurs in both sequences to yield the number ofmatched positions, dividing the number of matched positions by the totalnumber of positions in the window of comparison (i.e., the window size),and multiplying the result by 100 to yield the percentage of sequenceidentity. Included are nucleotides and polypeptides having at leastabout 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%,99% or 100% sequence identity to any of the reference sequencesdescribed herein, typically where the polypeptide variant maintains atleast one biological activity of the reference polypeptide.

Terms used to describe sequence relationships between two or morepolynucleotides or polypeptides include “reference sequence,”“comparison window,” “sequence identity,” “percentage of sequenceidentity,” and “substantial identity”. A “reference sequence” is atleast 12 but frequently 15 to 18 and often at least 25 monomer units,inclusive of nucleotides and amino acid residues, in length. Because twopolynucleotides may each comprise (1) a sequence (i.e., only a portionof the complete polynucleotide sequence) that is similar between the twopolynucleotides, and (2) a sequence that is divergent between the twopolynucleotides, sequence comparisons between two (or more)polynucleotides are typically performed by comparing sequences of thetwo polynucleotides over a “comparison window” to identify and comparelocal regions of sequence similarity. A “comparison window” refers to aconceptual segment of at least 6 contiguous positions, usually about 50to about 100, more usually about 100 to about 150 in which a sequence iscompared to a reference sequence of the same number of contiguouspositions after the two sequences are optimally aligned. The comparisonwindow may comprise additions or deletions (i.e., gaps) of about 20% orless as compared to the reference sequence (which does not compriseadditions or deletions) for optimal alignment of the two sequences.Optimal alignment of sequences for aligning a comparison window may beconducted by computerized implementations of algorithms (GAP, BESTFIT,FASTA, and TFASTA in for example, DNASTAR, GCG, DNA Strider, Geneious,Mac Vector, or Vector NTI software) or by inspection and the bestalignment (i.e., resulting in the highest percentage homology over thecomparison window) generated by any of the various methods selected.Reference also may be made to the BLAST family of programs as forexample disclosed by Altschul et al., 1997, Nucl. Acids Res. 25:3389. Adetailed discussion of sequence analysis can be found in Unit 19.3 ofAusubel et al., Current Protocols in Molecular Biology, John Wiley &Sons Inc., 1994-1998, Chapter 15.

An “isolated polynucleotide,” as used herein, refers to a polynucleotidethat has been purified from the sequences which flank it in anaturally-occurring state, e.g., a DNA fragment that has been removedfrom the sequences that are normally adjacent to the fragment. Inparticular embodiments, an “isolated polynucleotide” refers to acomplementary DNA (cDNA), a recombinant polynucleotide, a syntheticpolynucleotide, or other polynucleotide that does not exist in natureand that has been made by the hand of man.

In various embodiments, a polynucleotide comprises an mRNA encoding apolypeptide contemplated herein including, but not limited to, a homingendonuclease variant, a megaTAL, and an end-processing enzyme. Incertain embodiments, the mRNA comprises a cap, one or more nucleotides,and a poly(A) tail.

As used herein, the terms “5′ cap” or “5′ cap structure” or “5′ capmoiety” refer to a chemical modification, which has been incorporated atthe 5′ end of an mRNA. The 5′ cap is involved in nuclear export, mRNAstability, and translation.

In particular embodiments, a mRNA contemplated herein comprises a 5′ capcomprising a 5′-ppp-5′-triphosphate linkage between a terminal guanosinecap residue and the 5′-terminal transcribed sense nucleotide of the mRNAmolecule. This 5′-guanylate cap may then be methylated to generate anN7-methyl-guanylate residue.

Illustrative examples of 5′ cap suitable for use in particularembodiments of the mRNA polynucleotides contemplated herein include, butare not limited to: unmethylated 5′ cap analogs, e.g., G(5′)ppp(5′)G,G(5′)ppp(5′)C, G(5′)ppp(5′)A; methylated 5′ cap analogs, e.g.,m⁷G(5′)ppp(5′)G, m⁷G(5′)ppp(5′)C, and m⁷G(5′)ppp(5′)A; dimethylated 5′cap analogs, e.g., m^(2,7)G(5′)ppp(5′)G, m^(2,7)G(5′)ppp(5′)C, andm^(2,7)G(5′)ppp(5′)A; trimethylated 5′ cap analogs, e.g.,m^(2,2,7)G(5′)ppp(5′)G, m^(2,2,7)G(5′)ppp(5′)C, andm^(2,2,7)G(5′)ppp(5′)A; dimethylated symmetrical 5′ cap analogs, e.g.,m⁷G(5′)pppm⁷(5′)G, m⁷G(5′)pppm⁷(5′)C, and m⁷G(5′)pppm⁷(5′)A; andanti-reverse 5′ cap analogs, e.g, Anti-Reverse Cap Analog (ARCA) cap,designated 3′O-Me-m⁷G(5′)ppp(5′)G, 2′O-Me-m⁷G(5′)ppp(5′)G,2′O-Me-m⁷G(5′)ppp(5′)C, 2′O-Me-m⁷G(5′)ppp(5′)A, m⁷2′d(5′)ppp(5′)G,m⁷2′d(5′)ppp(5′)C, m⁷2′d(5′)ppp(5′)A, 3′O-Me-m⁷G(5′)ppp(5′)C,3′O-Me-m⁷G(5′)ppp(5′)A, m⁷3′d(5′)ppp(5′)G, m⁷3′d(5′)ppp(5′)C,m⁷3′d(5′)ppp(5′)A and their tetraphosphate derivatives) (see, e.g.,Jemielity et al., RNA, 9: 1108-1122 (2003)).

In particular embodiments, mRNAs comprise a 5′ cap that is a 7-methylguanylate (“m⁷G”) linked via a triphosphate bridge to the 5′-end of thefirst transcribed nucleotide, resulting in m⁷G-(5′)ppp(5′)N, where N isany nucleoside.

In some embodiments, mRNAs comprise a 5′ cap wherein the cap is a Cap0structure (Cap0 structures lack a 2′-O-methyl residue of the riboseattached to bases 1 and 2), a Cap1 structure (Cap1 structures have a2′-O-methyl residue at base 2), or a Cap2 structure (Cap2 structureshave a 2′-O-methyl residue attached to both bases 2 and 3).

In one embodiment, an mRNA comprises a m⁷G(5′)ppp(5′)G cap.

In one embodiment, an mRNA comprises an ARCA cap.

In particular embodiments, an mRNA contemplated herein comprises one ormore modified nucleosides.

In one embodiment, an mRNA comprises one or more modified nucleosidesselected from the group consisting of: pseudouridine, pyridin-4-oneribonucleoside, 5-aza-uridine, 2-thio-5-aza-uridine, 2-thiouridine,4-thio-pseudouridine, 2-thio-pseudouridine, 5-hydroxyuridine,3-methyluridine, 5-carboxymethyl-uridine, 1-carboxymethyl-pseudouridine,5-propynyl-uridine, 1-propynyl-pseudouridine, 5-taurinomethyluridine,1-taurinomethyl-pseudouridine, 5-taurinomethyl-2-thio-uridine,1-taurinomethyl-4-thio-uridine, 5-methyl-uridine,1-methyl-pseudouridine, 4-thio-1-methyl-pseudouridine,2-thio-1-methyl-pseudouridine, 1-methyl-1-deaza-pseudouridine,2-thio-1-methyl-1-deaza-pseudouridine, dihydrouridine,dihydropseudouridine, 2-thio-dihydrouridine,2-thio-dihydropseudouridine, 2-methoxyuridine, 2-methoxy-4-thio-uridine,4-methoxy-pseudouridine, 4-methoxy-2-thio-pseudouridine, 5-aza-cytidine,pseudoisocytidine, 3-methyl-cytidine, N4-acetylcytidine,5-formylcytidine, N4-methylcytidine, 5-hydroxymethylcytidine,1-methyl-pseudoisocytidine, pyrrolo-cytidine, pyrrolo-pseudoisocytidine,2-thio-cytidine, 2-thio-5-methyl-cytidine, 4-thio-pseudoisocytidine,4-thio-1-methyl-pseudoisocytidine,4-thio-1-methyl-1-deaza-pseudoisocytidine,1-methyl-1-deaza-pseudoisocytidine, zebularine, 5-aza-zebularine,5-methyl-zebularine, 5-aza-2-thio-zebularine, 2-thio-zebularine,2-methoxy-cytidine, 2-methoxy-5-methyl-cytidine,4-methoxy-pseudoisocytidine, 4-methoxy-1-methyl-pseudoisocytidine,2-aminopurine, 2,6-diaminopurine, 7-deaza-adenine,7-deaza-8-aza-adenine, 7-deaza-2-aminopurine,7-deaza-8-aza-2-aminopurine, 7-deaza-2,6-diaminopurine,7-deaza-8-aza-2,6-diaminopurine, 1-methyladenosine, N6-methyladenosine,N6-isopentenyladenosine, N6-(cis-hydroxyisopentenyl)adenosine,2-methylthio-N6-(cis-hydroxyisopentenyl) adenosine,N6-glycinylcarbamoyladenosine, N6-threonylcarbamoyladenosine,2-methylthio-N6-threonyl carbamoyladenosine, N6,N6-dimethyladenosine,7-methyladenine, 2-methylthio-adenine, 2-methoxy-adenine, inosine,1-methyl-inosine, wyosine, wybutosine, 7-deaza-guanosine,7-deaza-8-aza-guanosine, 6-thio-guanosine, 6-thio-7-deaza-guanosine,6-thio-7-deaza-8-aza-guanosine, 7-methyl-guanosine,6-thio-7-methyl-guanosine, 7-methylinosine, 6-methoxy-guanosine,1-methylguanosine, N2-methylguanosine, N2,N2-dimethylguanosine,8-oxo-guanosine, 7-methyl-8-oxo-guanosine, 1-methyl-6-thio-guanosine,N2-methyl-6-thio-guanosine, and N2,N2-dimethyl-6-thio-guanosine.

In one embodiment, an mRNA comprises one or more modified nucleosidesselected from the group consisting of: pseudouridine, pyridin-4-oneribonucleoside, 5-aza-uridine, 2-thio-5-aza-uridine, 2-thiouridine,4-thio-pseudouridine, 2-thio-pseudouridine, 5-hydroxyuridine,3-methyluridine, 5-carboxymethyl-uridine, 1-carboxymethyl-pseudouridine,5-propynyl-uridine, 1-propynyl-pseudouridine, 5-taurinomethyluridine,1-taurinomethyl-pseudouridine, 5-taurinomethyl-2-thio-uridine,1-taurinomethyl-4-thio-uridine, 5-methyl-uridine,1-methyl-pseudouridine, 4-thio-1-methyl-pseudouridine,2-thio-1-methyl-pseudouridine, 1-methyl-1-deaza-pseudouridine,2-thio-1-methyl-1-deaza-pseudouridine, dihydrouridine,dihydropseudouridine, 2-thio-dihydrouridine,2-thio-dihydropseudouridine, 2-methoxyuridine, 2-methoxy-4-thio-uridine,4-methoxy-pseudouridine, and 4-methoxy-2-thio-pseudouridine.

In one embodiment, an mRNA comprises one or more modified nucleosidesselected from the group consisting of: 5-aza-cytidine,pseudoisocytidine, 3-methyl-cytidine, N4-acetylcytidine,5-formylcytidine, N4-methylcytidine, 5-hydroxymethylcytidine,1-methyl-pseudoisocytidine, pyrrolo-cytidine, pyrrolo-pseudoisocytidine,2-thio-cytidine, 2-thio-5-methyl-cytidine, 4-thio-pseudoisocytidine,4-thio-1-methyl-pseudoisocytidine,4-thio-1-methyl-1-deaza-pseudoisocytidine,1-methyl-1-deaza-pseudoisocytidine, zebularine, 5-aza-zebularine,5-methyl-zebularine, 5-aza-2-thio-zebularine, 2-thio-zebularine,2-methoxy-cytidine, 2-methoxy-5-methyl-cytidine,4-methoxy-pseudoisocytidine, and 4-methoxy-1-methyl-pseudoisocytidine.

In one embodiment, an mRNA comprises one or more modified nucleosidesselected from the group consisting of: 2-aminopurine, 2,6-diaminopurine,7-deaza-adenine, 7-deaza-8-aza-adenine, 7-deaza-2-aminopurine,7-deaza-8-aza-2-aminopurine, 7-deaza-2,6-diaminopurine,7-deaza-8-aza-2,6-diaminopurine, 1-methyladenosine, N6-methyladenosine,N6-isopentenyladenosine, N6-(cis-hydroxyisopentenyl)adenosine,2-methylthio-N6-(cis-hydroxyisopentenyl) adenosine,N6-glycinylcarbamoyladenosine, N6-threonylcarbamoyladenosine,2-methylthio-N6-threonyl carbamoyladenosine, N6,N6-dimethyladenosine,7-methyladenine, 2-methylthio-adenine, and 2-methoxy-adenine.

In one embodiment, an mRNA comprises one or more modified nucleosidesselected from the group consisting of: inosine, 1-methyl-inosine,wyosine, wybutosine, 7-deaza-guanosine, 7-deaza-8-aza-guanosine,6-thio-guanosine, 6-thio-7-deaza-guanosine,6-thio-7-deaza-8-aza-guanosine, 7-methyl-guanosine,6-thio-7-methyl-guanosine, 7-methylinosine, 6-methoxy-guanosine,1-methylguanosine, N2-methylguanosine, N2,N2-dimethylguanosine,8-oxo-guanosine, 7-methyl-8-oxo-guanosine, 1-methyl-6-thio-guanosine,N2-methyl-6-thio-guanosine, and N2,N2-dimethyl-6-thio-guanosine.

In one embodiment, an mRNA comprises one or more pseudouridines, one ormore 5-methyl-cytosines, and/or one or more 5-methyl-cytidines.

In one embodiment, an mRNA comprises one or more pseudouridines.

In one embodiment, an mRNA comprises one or more 5-methyl-cytidines.

In one embodiment, an mRNA comprises one or more 5-methyl-cytosines.

In particular embodiments, an mRNA contemplated herein comprises apoly(A) tail to help protect the mRNA from exonuclease degradation,stabilize the mRNA, and facilitate translation. In certain embodiments,an mRNA comprises a 3′ poly(A) tail structure.

In particular embodiments, the length of the poly(A) tail is at leastabout 10, 25, 50, 75, 100, 150, 200, 250, 300, 350, 400, 450, or atleast about 500 or more adenine nucleotides or any intervening number ofadenine nucleotides. In particular embodiments, the length of thepoly(A) tail is at least about 125, 126, 127, 128, 129, 130, 131, 132,133, 134, 135, 136, 137, 138, 139, 140, 141, 142, 143, 144, 145, 146,147, 148, 149, 150, 151, 152, 153, 154, 155, 156, 157, 158, 159, 160,161, 162, 163, 164, 165, 166, 167, 168, 169, 170, 171, 172, 173, 174,175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188,189, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202,202, 203, 205, 206, 207, 208, 209, 210, 211, 212, 213, 214, 215, 216,217, 218, 219, 220, 221, 222, 223, 224, 225, 226, 227, 228, 229, 230,231, 232, 233, 234, 235, 236, 237, 238, 239, 240, 241, 242, 243, 244,245, 246, 247, 248, 249, 250, 251, 252, 253, 254, 255, 256, 257, 258,259, 260, 261, 262, 263, 264, 265, 266, 267, 268, 269, 270, 271, 272,273, 274, or 275 or more adenine nucleotides.

In particular embodiments, the length of the poly(A) tail is about 10 toabout 500 adenine nucleotides, about 50 to about 500 adeninenucleotides, about 100 to about 500 adenine nucleotides, about 150 toabout 500 adenine nucleotides, about 200 to about 500 adeninenucleotides, about 250 to about 500 adenine nucleotides, about 300 toabout 500 adenine nucleotides, about 50 to about 450 adeninenucleotides, about 50 to about 400 adenine nucleotides, about 50 toabout 350 adenine nucleotides, about 100 to about 500 adeninenucleotides, about 100 to about 450 adenine nucleotides, about 100 toabout 400 adenine nucleotides, about 100 to about 350 adeninenucleotides, about 100 to about 300 adenine nucleotides, about 150 toabout 500 adenine nucleotides, about 150 to about 450 adeninenucleotides, about 150 to about 400 adenine nucleotides, about 150 toabout 350 adenine nucleotides, about 150 to about 300 adeninenucleotides, about 150 to about 250 adenine nucleotides, about 150 toabout 200 adenine nucleotides, about 200 to about 500 adeninenucleotides, about 200 to about 450 adenine nucleotides, about 200 toabout 400 adenine nucleotides, about 200 to about 350 adeninenucleotides, about 200 to about 300 adenine nucleotides, about 250 toabout 500 adenine nucleotides, about 250 to about 450 adeninenucleotides, about 250 to about 400 adenine nucleotides, about 250 toabout 350 adenine nucleotides, or about 250 to about 300 adeninenucleotides or any intervening range of adenine nucleotides.

Terms that describe the orientation of polynucleotides include: 5′(normally the end of the polynucleotide having a free phosphate group)and 3′ (normally the end of the polynucleotide having a free hydroxyl(OH) group). Polynucleotide sequences can be annotated in the 5′ to 3′orientation or the 3′ to 5′ orientation. For DNA and mRNA, the 5′ to 3′strand is designated the “sense,” “plus,” or “coding” strand because itssequence is identical to the sequence of the pre-messenger (pre-mRNA)[except for uracil (U) in RNA, instead of thymine (T) in DNA]. For DNAand mRNA, the complementary 3′ to 5′ strand which is the strandtranscribed by the RNA polymerase is designated as “template,”“antisense,” “minus,” or “non-coding” strand. As used herein, the term“reverse orientation” refers to a 5′ to 3′ sequence written in the 3′ to5′ orientation or a 3′ to 5′ sequence written in the 5′ to 3′orientation.

The terms “complementary” and “complementarity” refer to polynucleotides(i.e., a sequence of nucleotides) related by the base-pairing rules. Forexample, the complementary strand of the DNA sequence 5′ AGTC AT G 3′ is3′ TCAGTAC 5′. The latter sequence is often written as the reversecomplement with the 5′ end on the left and the 3′ end on the right, 5′CAT GAC T 3′. A sequence that is equal to its reverse complement is saidto be a palindromic sequence. Complementarity can be “partial,” in whichonly some of the nucleic acid bases are matched according to the basepairing rules. Or, there can be “complete” or “total” complementaritybetween the nucleic acids.

The term “nucleic acid cassette” or “expression cassette” as used hereinrefers to genetic sequences within the vector which can express an RNA,and subsequently a polypeptide. In one embodiment, the nucleic acidcassette contains a gene(s)-of-interest, e.g., apolynucleotide(s)-of-interest. In another embodiment, the nucleic acidcassette contains one or more expression control sequences, e.g., apromoter, enhancer, poly(A) sequence, and a gene(s)-of-interest, e.g., apolynucleotide(s)-of-interest. Vectors may comprise 1, 2, 3, 4, 5, 6, 7,8, 9 or 10 or more nucleic acid cassettes. The nucleic acid cassette ispositionally and sequentially oriented within the vector such that thenucleic acid in the cassette can be transcribed into RNA, and whennecessary, translated into a protein or a polypeptide, undergoappropriate post-translational modifications required for activity inthe transformed cell, and be translocated to the appropriate compartmentfor biological activity by targeting to appropriate intracellularcompartments or secretion into extracellular compartments. Preferably,in some embodiments, the cassette has its 3′ and 5′ ends adapted forready insertion into a vector and/or genome, e.g., it has restrictionendonuclease sites at each end. In a preferred embodiment, the nucleicacid cassette contains the sequence of a therapeutic gene used to treat,prevent, or ameliorate a genetic disorder. The cassette can be removedand inserted into a plasmid or viral vector as a single unit.

Polynucleotides include polynucleotide(s)-of-interest. As used herein,the term “polynucleotide-of-interest” refers to a polynucleotideencoding a polypeptide or fusion polypeptide or a polynucleotide thatserves as a template for the transcription of an inhibitorypolynucleotide, as contemplated herein.

Moreover, it will be appreciated by those of ordinary skill in the artthat, as a result of the degeneracy of the genetic code, there are manynucleotide sequences that may encode a polypeptide, or fragment ofvariant thereof, as contemplated herein. Some of these polynucleotidesbear minimal homology to the nucleotide sequence of any native gene.Nonetheless, polynucleotides that vary due to differences in codon usageare specifically contemplated in particular embodiments, for examplepolynucleotides that are optimized for human and/or primate codonselection. In one embodiment, polynucleotides comprising particularallelic sequences are provided. Alleles are endogenous polynucleotidesequences that are altered as a result of one or more mutations, such asdeletions, additions and/or substitutions of nucleotides.

In a certain embodiment, a polynucleotide-of-interest comprises a donorrepair template.

In a certain embodiment, a polynucleotide-of-interest comprises aninhibitory polynucleotide including, but not limited to, an siRNA, anmiRNA, an shRNA, a ribozyme or another inhibitory RNA.

In one embodiment, a donor repair template comprising an inhibitory RNAcomprises one or more regulatory sequences, such as, for example, astrong constitutive pol III, e.g., human or mouse U6 snRNA promoter, thehuman and mouse H1 RNA promoter, or the human tRNA-val promoter, or astrong constitutive pol II promoter, as described elsewhere herein.

The polynucleotides contemplated in particular embodiments, regardlessof the length of the coding sequence itself, may be combined with otherDNA sequences, such as promoters and/or enhancers, untranslated regions(UTRs), Kozak sequences, polyadenylation signals, additional restrictionenzyme sites, multiple cloning sites, internal ribosomal entry sites(IRES), recombinase recognition sites (e.g., LoxP, FRT, and Att sites),termination codons, transcriptional termination signals,post-transcription response elements, and polynucleotides encodingself-cleaving polypeptides, epitope tags, as disclosed elsewhere hereinor as known in the art, such that their overall length may varyconsiderably. It is therefore contemplated in particular embodimentsthat a polynucleotide fragment of almost any length may be employed,with the total length preferably being limited by the ease ofpreparation and use in the intended recombinant DNA protocol.

Polynucleotides can be prepared, manipulated, expressed and/or deliveredusing any of a variety of well-established techniques known andavailable in the art. In order to express a desired polypeptide, anucleotide sequence encoding the polypeptide, can be inserted intoappropriate vector. A desired polypeptide can also be expressed bydelivering an mRNA encoding the polypeptide into the cell.

Illustrative examples of vectors include, but are not limited toplasmid, autonomously replicating sequences, and transposable elements,e.g., Sleeping Beauty, PiggyBac.

Additional illustrative examples of vectors include, without limitation,plasmids, phagemids, cosmids, artificial chromosomes such as yeastartificial chromosome (YAC), bacterial artificial chromosome (BAC), orP1-derived artificial chromosome (PAC), bacteriophages such as lambdaphage or M13 phage, and animal viruses.

Illustrative examples of viruses useful as vectors include, withoutlimitation, retrovirus (including lentivirus), adenovirus,adeno-associated virus, herpesvirus (e.g., herpes simplex virus),poxvirus, baculovirus, papillomavirus, and papovavirus (e.g., SV40).

Illustrative examples of expression vectors include, but are not limitedto pClneo vectors (Promega) for expression in mammalian cells;pLenti4N5-DEST™, pLenti6/V5-DEST™, and pLenti6.2/V5-GW/lacZ (Invitrogen)for lentivirus-mediated gene transfer and expression in mammalian cells.In particular embodiments, coding sequences of polypeptides disclosedherein can be ligated into such expression vectors for the expression ofthe polypeptides in mammalian cells.

In particular embodiments, the vector is an episomal vector or a vectorthat is maintained extrachromosomally. As used herein, the term“episomal” refers to a vector that is able to replicate withoutintegration into host's chromosomal DNA and without gradual loss from adividing host cell also meaning that said vector replicatesextrachromosomally or episomally.

“Expression control sequences,” “control elements,” or “regulatorysequences” present in an expression vector are those non-translatedregions of the vector—origin of replication, selection cassettes,promoters, enhancers, translation initiation signals (Shine Dalgarnosequence or Kozak sequence) introns, post-transcriptional regulatoryelements, a polyadenylation sequence, 5′ and 3′ untranslatedregions—which interact with host cellular proteins to carry outtranscription and translation. Such elements may vary in their strengthand specificity. Depending on the vector system and host utilized, anynumber of suitable transcription and translation elements, includingubiquitous promoters and inducible promoters may be used.

In particular embodiments, a polynucleotide comprises a vector,including but not limited to expression vectors and viral vectors. Avector may comprise one or more exogenous, endogenous, or heterologouscontrol sequences such as promoters and/or enhancers. An “endogenouscontrol sequence” is one which is naturally linked with a given gene inthe genome. An “exogenous control sequence” is one which is placed injuxtaposition to a gene by means of genetic manipulation (i.e.,molecular biological techniques) such that transcription of that gene isdirected by the linked enhancer/promoter. A “heterologous controlsequence” is an exogenous sequence that is from a different species thanthe cell being genetically manipulated. A “synthetic” control sequencemay comprise elements of one more endogenous and/or exogenous sequences,and/or sequences determined in vitro or in silico that provide optimalpromoter and/or enhancer activity for the particular therapy.

The term “promoter” as used herein refers to a recognition site of apolynucleotide (DNA or RNA) to which an RNA polymerase binds. An RNApolymerase initiates and transcribes polynucleotides operably linked tothe promoter. In particular embodiments, promoters operative inmammalian cells comprise an AT-rich region located approximately 25 to30 bases upstream from the site where transcription is initiated and/oranother sequence found 70 to 80 bases upstream from the start oftranscription, a CNCAAT region where N may be any nucleotide.

The term “enhancer” refers to a segment of DNA which contains sequencescapable of providing enhanced transcription and in some instances canfunction independent of their orientation relative to another controlsequence. An enhancer can function cooperatively or additively withpromoters and/or other enhancer elements. The term “promoter/enhancer”refers to a segment of DNA which contains sequences capable of providingboth promoter and enhancer functions.

The term “operably linked”, refers to a juxtaposition wherein thecomponents described are in a relationship permitting them to functionin their intended manner. In one embodiment, the term refers to afunctional linkage between a nucleic acid expression control sequence(such as a promoter, and/or enhancer) and a second polynucleotidesequence, e.g., a polynucleotide-of-interest, wherein the expressioncontrol sequence directs transcription of the nucleic acid correspondingto the second sequence.

As used herein, the term “constitutive expression control sequence”refers to a promoter, enhancer, or promoter/enhancer that continually orcontinuously allows for transcription of an operably linked sequence. Aconstitutive expression control sequence may be a “ubiquitous” promoter,enhancer, or promoter/enhancer that allows expression in a wide varietyof cell and tissue types or a “cell specific,” “cell type specific,”“cell lineage specific,” or “tissue specific” promoter, enhancer, orpromoter/enhancer that allows expression in a restricted variety of celland tissue types, respectively.

Illustrative ubiquitous expression control sequences suitable for use inparticular embodiments include, but are not limited to, acytomegalovirus (CMV) immediate early promoter, a viral simian virus 40(SV40) (e.g., early or late), a Moloney murine leukemia virus (MoMLV)LTR promoter, a Rous sarcoma virus (RSV) LTR, a herpes simplex virus(HSV) (thymidine kinase) promoter, H5, P7.5, and P11 promoters fromvaccinia virus, a short elongation factor 1-alpha (EF1a-short) promoter,a long elongation factor 1-alpha (EF1a-long) promoter, early growthresponse 1 (EGR1), ferritin H (FerH), ferritin L (FerL), Glyceraldehyde3-phosphate dehydrogenase (GAPDH), eukaryotic translation initiationfactor 4A1 (EIF4A1), heat shock 70 kDa protein 5 (HSPA5), heat shockprotein 90 kDa beta, member 1 (HSP90B1), heat shock protein 70 kDa(HSP70), β-kinesin (β-KIN), the human ROSA 26 locus (Irions et al.,Nature Biotechnology 25, 1477-1482 (2007)), a Ubiquitin C promoter(UBC), a phosphoglycerate kinase-1 (PGK) promoter, a cytomegalovirusenhancer/chicken β-actin (CAG) promoter, a β-actin promoter and amyeloproliferative sarcoma virus enhancer, negative control regiondeleted, dl587rev primer-binding site substituted (MND) promoter(Challita et al., J Virol. 69(2):748-55 (1995)).

In a particular embodiment, it may be desirable to use a cell, celltype, cell lineage or tissue specific expression control sequence toachieve cell type specific, lineage specific, or tissue specificexpression of a desired polynucleotide sequence (e.g., to express aparticular nucleic acid encoding a polypeptide in only a subset of celltypes, cell lineages, or tissues or during specific stages ofdevelopment).

As used herein, “conditional expression” may refer to any type ofconditional expression including, but not limited to, inducibleexpression; repressible expression; expression in cells or tissueshaving a particular physiological, biological, or disease state, etc.This definition is not intended to exclude cell type or tissue specificexpression. Certain embodiments provide conditional expression of apolynucleotide-of-interest, e.g., expression is controlled by subjectinga cell, tissue, organism, etc., to a treatment or condition that causesthe polynucleotide to be expressed or that causes an increase ordecrease in expression of the polynucleotide encoded by thepolynucleotide-of-interest.

Illustrative examples of inducible promoters/systems include, but arenot limited to, steroid-inducible promoters such as promoters for genesencoding glucocorticoid or estrogen receptors (inducible by treatmentwith the corresponding hormone), metallothionine promoter (inducible bytreatment with various heavy metals), MX-1 promoter (inducible byinterferon), the “GeneSwitch” mifepristone-regulatable system (Sirin etal., 2003, Gene, 323:67), the cumate inducible gene switch (WO2002/088346), tetracycline-dependent regulatory systems, etc.

Conditional expression can also be achieved by using a site specific DNArecombinase. According to certain embodiments, polynucleotides comprisesat least one (typically two) site(s) for recombination mediated by asite specific recombinase. As used herein, the terms “recombinase” or“site specific recombinase” include excisive or integrative proteins,enzymes, co-factors or associated proteins that are involved inrecombination reactions involving one or more recombination sites (e.g.,two, three, four, five, six, seven, eight, nine, ten or more.), whichmay be wild-type proteins (see Landy, Current Opinion in Biotechnology3:699-707 (1993)), or mutants, derivatives (e.g., fusion proteinscontaining the recombination protein sequences or fragments thereof),fragments, and variants thereof. Illustrative examples of recombinasessuitable for use in particular embodiments include, but are not limitedto: Cre, Int, IHF, Xis, Flp, Fis, Hin, Gin, ΦC31, Cin, Tn3 resolvase,TndX, XerC, XerD, TnpX, Hjc, Gin, SpCCE1, and ParA.

The polynucleotides may comprise one or more recombination sites for anyof a wide variety of site specific recombinases. It is to be understoodthat the target site for a site specific recombinase is in addition toany site(s) required for integration of a vector, e.g., a retroviralvector or lentiviral vector. As used herein, the terms “recombinationsequence,” “recombination site,” or “site specific recombination site”refer to a particular nucleic acid sequence to which a recombinaserecognizes and binds.

For example, one recombination site for Cre recombinase is loxP which isa 34 base pair sequence comprising two 13 base pair inverted repeats(serving as the recombinase binding sites) flanking an 8 base pair coresequence (Sauer, B., Current Opinion in Biotechnology 5:521-527 (1994)).Other exemplary loxP sites include, but are not limited to: lox511(Hoess et al., 1996; Bethke and Sauer, 1997), lox5171 (Lee and Saito,1998), lox2272 (Lee and Saito, 1998), m2 (Langer et al., 2002), lox71(Albert et al., 1995), and lox66 (Albert et al., 1995).

Suitable recognition sites for the FLP recombinase include, but are notlimited to: FRT (McLeod, et al., 1996), F₁, F₂, F₃ (Schlake and Bode,1994), F₄, F₅ (Schlake and Bode, 1994), FRT(LE) (Senecoff et al., 1988),FRT(RE) (Senecoff et al., 1988).

Other examples of recognition sequences are the attB, attP, attL, andattR sequences, which are recognized by the recombinase enzyme λIntegrase, e.g., phi-c31. The φC31 SSR mediates recombination onlybetween the heterotypic sites attB (34 bp in length) and attP (39 bp inlength) (Groth et al., 2000). attB and attP, named for the attachmentsites for the phage integrase on the bacterial and phage genomes,respectively, both contain imperfect inverted repeats that are likelybound by φC31 homodimers (Groth et al., 2000). The product sites, attLand attR, are effectively inert to further φC31-mediated recombination(Belteki et al., 2003), making the reaction irreversible. For catalyzinginsertions, it has been found that attB-bearing DNA inserts into agenomic attP site more readily than an attP site into a genomic attBsite (Thyagarajan et al., 2001; Belteki et al., 2003). Thus, typicalstrategies position by homologous recombination an attP-bearing “dockingsite” into a defined locus, which is then partnered with an attB-bearingincoming sequence for insertion.

In one embodiment, a polynucleotide contemplated herein comprises adonor repair template polynucleotide flanked by a pair of recombinaserecognition sites. In particular embodiments, the repair templatepolynucleotide is flanked by LoxP sites, FRT sites, or att sites.

In particular embodiments, polynucleotides contemplated herein, includeone or more polynucleotides-of-interest that encode one or morepolypeptides. In particular embodiments, to achieve efficienttranslation of each of the plurality of polypeptides, the polynucleotidesequences can be separated by one or more IRES sequences orpolynucleotide sequences encoding self-cleaving polypeptides.

As used herein, an “internal ribosome entry site” or “IRES” refers to anelement that promotes direct internal ribosome entry to the initiationcodon, such as ATG, of a cistron (a protein encoding region), therebyleading to the cap-independent translation of the gene. See, e.g.,Jackson et al., 1990. Trends Biochem Sci 15(12):477-83) and Jackson andKaminski. 1995. RNA 1(10):985-1000. Examples of IRES generally employedby those of skill in the art include those described in U.S. Pat. No.6,692,736. Further examples of “IRES” known in the art include, but arenot limited to IRES obtainable from picornavirus (Jackson et al., 1990)and IRES obtainable from viral or cellular mRNA sources, such as forexample, immunoglobulin heavy-chain binding protein (BiP), the vascularendothelial growth factor (VEGF) (Huez et al. 1998. Mol. Cell. Biol.18(11):6178-6190), the fibroblast growth factor 2 (FGF-2), andinsulin-like growth factor (IGFII), the translational initiation factoreIF4G and yeast transcription factors TFIID and HAP4, theencephelomycarditis virus (EMCV) which is commercially available fromNovagen (Duke et al., 1992. J. Virol 66(3):1602-9) and the VEGF IRES(Huez et al., 1998. Mol Cell Biol 18(11):6178-90). IRES have also beenreported in viral genomes of Picornaviridae, Dicistroviridae andFlaviviridae species and in HCV, Friend murine leukemia virus (FrMLV)and Moloney murine leukemia virus (MoMLV).

In one embodiment, the IRES used in polynucleotides contemplated hereinis an EMCV IRES.

In particular embodiments, the polynucleotides comprise polynucleotidesthat have a consensus Kozak sequence and that encode a desiredpolypeptide. As used herein, the term “Kozak sequence” refers to a shortnucleotide sequence that greatly facilitates the initial binding of mRNAto the small subunit of the ribosome and increases translation. Theconsensus Kozak sequence is (GCC)RCCATGG (SEQ ID NO:75), where R is apurine (A or G) (Kozak, 1986. Cell. 44(2):283-92, and Kozak, 1987.Nucleic Acids Res. 15(20):8125-48).

Elements directing the efficient termination and polyadenylation of theheterologous nucleic acid transcripts increases heterologous geneexpression. Transcription termination signals are generally founddownstream of the polyadenylation signal. In particular embodiments,vectors comprise a polyadenylation sequence 3′ of a polynucleotideencoding a polypeptide to be expressed. The term “polyA site” or “polyAsequence” as used herein denotes a DNA sequence which directs both thetermination and polyadenylation of the nascent RNA transcript by RNApolymerase II. Polyadenylation sequences can promote mRNA stability byaddition of a polyA tail to the 3′ end of the coding sequence and thus,contribute to increased translational efficiency. Cleavage andpolyadenylation is directed by a poly(A) sequence in the RNA. The corepoly(A) sequence for mammalian pre-mRNAs has two recognition elementsflanking a cleavage-polyadenylation site. Typically, an almost invariantAAUAAA hexamer lies 20-50 nucleotides upstream of a more variableelement rich in U or GU residues. Cleavage of the nascent transcriptoccurs between these two elements and is coupled to the addition of upto 250 adenosines to the 5′ cleavage product. In particular embodiments,the core poly(A) sequence is an ideal polyA sequence (e.g., AATAAA,ATTAAA, AGTAAA). In particular embodiments, the poly(A) sequence is anSV40 polyA sequence, a bovine growth hormone polyA sequence (BGHpA), arabbit β-globin polyA sequence (rβgpA), variants thereof, or anothersuitable heterologous or endogenous polyA sequence known in the art.

In some embodiments, a polynucleotide or cell harboring thepolynucleotide utilizes a suicide gene, including an inducible suicidegene to reduce the risk of direct toxicity and/or uncontrolledproliferation. In specific embodiments, the suicide gene is notimmunogenic to the host harboring the polynucleotide or cell. A certainexample of a suicide gene that may be used is caspase-9 or caspase-8 orcytosine deaminase. Caspase-9 can be activated using a specific chemicalinducer of dimerization (CID).

In certain embodiments, polynucleotides comprise gene segments thatcause the genetically modified cells contemplated herein to besusceptible to negative selection in vivo. “Negative selection” refersto an infused cell that can be eliminated as a result of a change in thein vivo condition of the individual. The negative selectable phenotypemay result from the insertion of a gene that confers sensitivity to anadministered agent, for example, a compound. Negative selection genesare known in the art, and include, but are not limited to: the Herpessimplex virus type I thymidine kinase (HSV-I TK) gene which confersganciclovir sensitivity; the cellular hypoxanthinephosphribosyltransferase (HPRT) gene, the cellular adeninephosphoribosyltransferase (APRT) gene, and bacterial cytosine deaminase.

In some embodiments, genetically modified cells comprise apolynucleotide further comprising a positive marker that enables theselection of cells of the negative selectable phenotype in vitro. Thepositive selectable marker may be a gene, which upon being introducedinto the host cell, expresses a dominant phenotype permitting positiveselection of cells carrying the gene. Genes of this type are known inthe art, and include, but are not limited to hygromycin-Bphosphotransferase gene (hph) which confers resistance to hygromycin B,the amino glycoside phosphotransferase gene (neo or aph) from Tn5 whichcodes for resistance to the antibiotic G418, the dihydrofolate reductase(DHFR) gene, the adenosine deaminase gene (ADA), and the multi-drugresistance (MDR) gene.

In one embodiment, the positive selectable marker and the negativeselectable element are linked such that loss of the negative selectableelement necessarily also is accompanied by loss of the positiveselectable marker. In a particular embodiment, the positive and negativeselectable markers are fused so that loss of one obligatorily leads toloss of the other. An example of a fused polynucleotide that yields asan expression product a polypeptide that confers both the desiredpositive and negative selection features described above is a hygromycinphosphotransferase thymidine kinase fusion gene (HyTK). Expression ofthis gene yields a polypeptide that confers hygromycin B resistance forpositive selection in vitro, and ganciclovir sensitivity for negativeselection in vivo. See also the publications of PCT US91/08442 andPCT/US94/05601, by S. D. Lupton, describing the use of bifunctionalselectable fusion genes derived from fusing a dominant positiveselectable markers with negative selectable markers.

Preferred positive selectable markers are derived from genes selectedfrom the group consisting of hph, nco, and gpt, and preferred negativeselectable markers are derived from genes selected from the groupconsisting of cytosine deaminase, HSV-I TK, VZV TK, HPRT, APRT and gpt.Exemplary bifunctional selectable fusion genes contemplated inparticular embodiments include, but are not limited to genes wherein thepositive selectable marker is derived from hph or neo, and the negativeselectable marker is derived from cytosine deaminase or a TK gene orselectable marker.

In particular embodiments, polynucleotides encoding one or more nucleasevariants, megaTALs, end-processing enzymes, or fusion polypeptides maybe introduced into hematopoietic cells, e.g., T cells, by both non-viraland viral methods. In particular embodiments, delivery of one or morepolynucleotides encoding nucleases and/or donor repair templates may beprovided by the same method or by different methods, and/or by the samevector or by different vectors.

The term “vector” is used herein to refer to a nucleic acid moleculecapable transferring or transporting another nucleic acid molecule. Thetransferred nucleic acid is generally linked to, e.g., inserted into,the vector nucleic acid molecule. A vector may include sequences thatdirect autonomous replication in a cell, or may include sequencessufficient to allow integration into host cell DNA. In particularembodiments, non-viral vectors are used to deliver one or morepolynucleotides contemplated herein to a T cell.

Illustrative examples of non-viral vectors include, but are not limitedto plasmids (e.g., DNA plasmids or RNA plasmids), transposons, cosmids,and bacterial artificial chromosomes.

Illustrative methods of non-viral delivery of polynucleotidescontemplated in particular embodiments include, but are not limited to:electroporation, sonoporation, lipofection, microinjection, biolistics,virosomes, liposomes, immunoliposomes, nanoparticles, polycation orlipid:nucleic acid conjugates, naked DNA, artificial virions,DEAE-dextran-mediated transfer, gene gun, and heat-shock.

Illustrative examples of polynucleotide delivery systems suitable foruse in particular embodiments contemplated in particular embodimentsinclude, but are not limited to those provided by Amaxa Biosystems,Maxcyte, Inc., BTX Molecular Delivery Systems, and CopernicusTherapeutics Inc. Lipofection reagents are sold commercially (e.g.,Transfectam™ and Lipofectin™). Cationic and neutral lipids that aresuitable for efficient receptor-recognition lipofection ofpolynucleotides have been described in the literature. See e.g., Liu etal. (2003) Gene Therapy. 10:180-187; and Balazs et al. (2011) Journal ofDrug Delivery. 2011:1-12. Antibody-targeted, bacterially derived,non-living nanocell-based delivery is also contemplated in particularembodiments.

Viral vectors comprising polynucleotides contemplated in particularembodiments can be delivered in vivo by administration to an individualpatient, typically by systemic administration (e.g., intravenous,intraperitoneal, intramuscular, subdermal, or intracranial infusion) ortopical application, as described below. Alternatively, vectors can bedelivered to cells ex vivo, such as cells explanted from an individualpatient (e.g., mobilized peripheral blood, lymphocytes, bone marrowaspirates, tissue biopsy, etc.) or universal donor hematopoietic stemcells, followed by reimplantation of the cells into a patient.

In one embodiment, viral vectors comprising nuclease variants and/ordonor repair templates are administered directly to an organism fortransduction of cells in vivo. Alternatively, naked DNA can beadministered. Administration is by any of the routes normally used forintroducing a molecule into ultimate contact with blood or tissue cellsincluding, but not limited to, injection, infusion, topical applicationand electroporation. Suitable methods of administering such nucleicacids are available and well known to those of skill in the art, and,although more than one route can be used to administer a particularcomposition, a particular route can often provide a more immediate andmore effective reaction than another route.

Illustrative examples of viral vector systems suitable for use inparticular embodiments contemplated herein include, but are not limitedto adeno-associated virus (AAV), retrovirus, herpes simplex virus,adenovirus, and vaccinia virus vectors.

In various embodiments, one or more polynucleotides encoding a nucleasevariant and/or donor repair template are introduced into a hematopoieticcell, e.g., a T cell, by transducing the cell with a recombinantadeno-associated virus (rAAV), comprising the one or morepolynucleotides.

AAV is a small (˜26 nm) replication-defective, primarily episomal,non-enveloped virus. AAV can infect both dividing and non-dividing cellsand may incorporate its genome into that of the host cell. RecombinantAAV (rAAV) are typically composed of, at a minimum, a transgene and itsregulatory sequences, and 5′ and 3′ AAV inverted terminal repeats(ITRs). The ITR sequences are about 145 bp in length. In particularembodiments, the rAAV comprises ITRs and capsid sequences isolated fromAAV1, AAV2, AAV3, AAV4, AAV5, AAV6, AAV7, AAV8, AAV9, or AAV10.

In some embodiments, a chimeric rAAV is used the ITR sequences areisolated from one AAV serotype and the capsid sequences are isolatedfrom a different AAV serotype. For example, a rAAV with ITR sequencesderived from AAV2 and capsid sequences derived from AAV6 is referred toas AAV2/AAV6. In particular embodiments, the rAAV vector may compriseITRs from AAV2, and capsid proteins from any one of AAV1, AAV2, AAV3,AAV4, AAV5, AAV6, AAV7, AAV8, AAV9, or AAV10. In a preferred embodiment,the rAAV comprises ITR sequences derived from AAV2 and capsid sequencesderived from AAV6. In a preferred embodiment, the rAAV comprises ITRsequences derived from AAV2 and capsid sequences derived from AAV2.

In some embodiments, engineering and selection methods can be applied toAAV capsids to make them more likely to transduce cells of interest.

Construction of rAAV vectors, production, and purification thereof havebeen disclosed, e.g., in U.S. Pat. Nos. 9,169,494; 9,169,492; 9,012,224;8,889,641; 8,809,058; and 8,784,799, each of which is incorporated byreference herein, in its entirety.

In various embodiments, one or more polynucleotides encoding a nucleasevariant and/or donor repair template are introduced into a hematopoieticcell, by transducing the cell with a retrovirus, e.g., lentivirus,comprising the one or more polynucleotides.

As used herein, the term “retrovirus” refers to an RNA virus thatreverse transcribes its genomic RNA into a linear double-stranded DNAcopy and subsequently covalently integrates its genomic DNA into a hostgenome. Illustrative retroviruses suitable for use in particularembodiments, include, but are not limited to: Moloney murine leukemiavirus (M-MuLV), Moloney murine sarcoma virus (MoMSV), Harvey murinesarcoma virus (HaMuSV), murine mammary tumor virus (MuMTV), gibbon apeleukemia virus (GaLV), feline leukemia virus (FLV), spumavirus, Friendmurine leukemia virus, Murine Stem Cell Virus (MSCV) and Rous SarcomaVirus (RSV)) and lentivirus.

As used herein, the term “lentivirus” refers to a group (or genus) ofcomplex retroviruses. Illustrative lentiviruses include, but are notlimited to: HIV (human immunodeficiency virus; including HIV type 1, andHIV 2); visna-maedi virus (VMV) virus; the caprinearthritis-encephalitis virus (CAEV); equine infectious anemia virus(EIAV); feline immunodeficiency virus (FIV); bovine immune deficiencyvirus (BIV); and simian immunodeficiency virus (SIV). In one embodiment,HIV based vector backbones (i.e., HIV cis-acting sequence elements) arepreferred.

In various embodiments, a lentiviral vector contemplated hereincomprises one or more LTRs, and one or more, or all, of the followingaccessory elements: a cPPT/FLAP, a Psi (Ψ) packaging signal, an exportelement, poly (A) sequences, and may optionally comprise a WPRE or HPRE,an insulator element, a selectable marker, and a cell suicide gene, asdiscussed elsewhere herein.

In particular embodiments, lentiviral vectors contemplated herein may beintegrative or non-integrating or integration defective lentivirus. Asused herein, the term “integration defective lentivirus” or “IDLV”refers to a lentivirus having an integrase that lacks the capacity tointegrate the viral genome into the genome of the host cells.Integration-incompetent viral vectors have been described in patentapplication WO 2006/010834, which is herein incorporated by reference inits entirety.

Illustrative mutations in the HIV-1 pol gene suitable to reduceintegrase activity include, but are not limited to: H12N, H12C, H16C,H16V, S81R, D41A, K42A, H51A, Q53C, D55V, D64E, D64V, E69A, K71A, E85A,E87A, D116N, D1161, D116A, N120G, N1201, N120E, E152G, E152A, D35E,K156E, K156A, E157A, K159E, K159A, K160A, R166A, D167A, E170A, H171A,K173A, K186Q, K186T, K188T, E198A, R199c, R199T, R199A, D202A, K211A,Q214L, Q216L, Q221L, W235F, W235E, K236S, K236A, K246A, G247W, D253A,R262A, R263A and K264H.

In one embodiment, the HIV-1 integrase deficient pol gene comprises aD64V, D116I, D116A, E152G, or E152A mutation; D64V, D116I, and E152Gmutations; or D64V, D116A, and E152A mutations.

In one embodiment, the HIV-1 integrase deficient pol gene comprises aD64V mutation.

The term “long terminal repeat (LTR)” refers to domains of base pairslocated at the ends of retroviral DNAs which, in their natural sequencecontext, are direct repeats and contain U3, R and U5 regions.

As used herein, the term “FLAP element” or “cPPT/FLAP” refers to anucleic acid whose sequence includes the central polypurine tract andcentral termination sequences (cPPT and CTS) of a retrovirus, e.g.,HIV-1 or HIV-2. Suitable FLAP elements are described in U.S. Pat. No.6,682,907 and in Zennou, et al., 2000, Cell, 101:173. In anotherembodiment, a lentiviral vector contains a FLAP element with one or moremutations in the cPPT and/or CTS elements. In yet another embodiment, alentiviral vector comprises either a cPPT or CTS element. In yet anotherembodiment, a lentiviral vector does not comprise a cPPT or CTS element.

As used herein, the term “packaging signal” or “packaging sequence”refers to psi [Ψ] sequences located within the retroviral genome whichare required for insertion of the viral RNA into the viral capsid orparticle, see e.g., Clever et al., 1995. J. of Virology, Vol. 69, No. 4;pp. 2101-2109.

The term “export element” refers to a cis-acting post-transcriptionalregulatory element which regulates the transport of an RNA transcriptfrom the nucleus to the cytoplasm of a cell. Examples of RNA exportelements include, but are not limited to, the human immunodeficiencyvirus (HIV) rev response element (RRE) (see e.g., Cullen et al., 1991.J. Virol. 65: 1053; and Cullen et al., 1991. Cell 58: 423), and thehepatitis B virus post-transcriptional regulatory element (HPRE).

In particular embodiments, expression of heterologous sequences in viralvectors is increased by incorporating posttranscriptional regulatoryelements, efficient polyadenylation sites, and optionally, transcriptiontermination signals into the vectors. A variety of posttranscriptionalregulatory elements can increase expression of a heterologous nucleicacid at the protein, e.g., woodchuck hepatitis virus posttranscriptionalregulatory element (WPRE; Zufferey et al., 1999, J. Virol., 73:2886);the posttranscriptional regulatory element present in hepatitis B virus(HPRE) (Huang et al., Mol. Cell. Biol., 5:3864); and the like (Liu etal., 1995, Genes Dev., 9:1766).

Lentiviral vectors preferably contain several safety enhancements as aresult of modifying the LTRs. “Self-inactivating” (SIN) vectors refersto replication-defective vectors, e.g., in which the right (3′) LTRenhancer-promoter region, known as the U3 region, has been modified(e.g., by deletion or substitution) to prevent viral transcriptionbeyond the first round of viral replication. An additional safetyenhancement is provided by replacing the U3 region of the 5′ LTR with aheterologous promoter to drive transcription of the viral genome duringproduction of viral particles. Examples of heterologous promoters whichcan be used include, for example, viral simian virus 40 (SV40) (e.g.,early or late), cytomegalovirus (CMV) (e.g., immediate early), Moloneymurine leukemia virus (MoMLV), Rous sarcoma virus (RSV), and herpessimplex virus (HSV) (thymidine kinase) promoters.

The terms “pseudotype” or “pseudotyping” as used herein, refer to avirus whose viral envelope proteins have been substituted with those ofanother virus possessing preferable characteristics. For example, HIVcan be pseudotyped with vesicular stomatitis virus G-protein (VSV-G)envelope proteins, which allows HIV to infect a wider range of cellsbecause HIV envelope proteins (encoded by the env gene) normally targetthe virus to CD4⁺ presenting cells.

In certain embodiments, lentiviral vectors are produced according toknown methods. See e.g., Kutner et al., BMC Biotechnol. 2009; 9:10. doi:10.1186/1472-6750-9-10; Kutner et al. Nat. Protoc. 2009; 4(4):495-505.doi: 10.1038/nprot.2009.22.

According to certain specific embodiments contemplated herein, most orall of the viral vector backbone sequences are derived from alentivirus, e.g., HIV-1. However, it is to be understood that manydifferent sources of retroviral and/or lentiviral sequences can be used,or combined and numerous substitutions and alterations in certain of thelentiviral sequences may be accommodated without impairing the abilityof a transfer vector to perform the functions described herein.Moreover, a variety of lentiviral vectors are known in the art, seeNaldini et al., (1996a, 1996b, and 1998); Zufferey et al., (1997); Dullet al., 1998, U.S. Pat. Nos. 6,013,516; and 5,994,136, many of which maybe adapted to produce a viral vector or transfer plasmid contemplatedherein.

In various embodiments, one or more polynucleotides encoding a nucleasevariant and/or donor repair template are introduced into a hematopoieticcell by transducing the cell with an adenovirus comprising the one ormore polynucleotides.

Adenoviral based vectors are capable of very high transductionefficiency in many cell types and do not require cell division. Withsuch vectors, high titer and high levels of expression have beenobtained. This vector can be produced in large quantities in arelatively simple system. Most adenovirus vectors are engineered suchthat a transgene replaces the Ad E1a, E1b, and/or E3 genes; subsequentlythe replication defective vector is propagated in human 293 cells thatsupply deleted gene function in trans. Ad vectors can transduce multipletypes of tissues in vivo, including non-dividing, differentiated cellssuch as those found in liver, kidney and muscle. Conventional Ad vectorshave a large carrying capacity.

Generation and propagation of the current adenovirus vectors, which arereplication deficient, may utilize a unique helper cell line, designated293, which was transformed from human embryonic kidney cells by Ad5 DNAfragments and constitutively expresses E1 proteins (Graham et al.,1977). Since the E3 region is dispensable from the adenovirus genome(Jones & Shenk, 1978), the current adenovirus vectors, with the help of293 cells, carry foreign DNA in either the E1, the D3 or both regions(Graham & Prevec, 1991). Adenovirus vectors have been used in eukaryoticgene expression (Levrero et al., 1991; Gomez-Foix et al., 1992) andvaccine development (Grunhaus & Horwitz, 1992; Graham & Prevec, 1992).Studies in administering recombinant adenovirus to different tissuesinclude trachea instillation (Rosenfeld et al., 1991; Rosenfeld et al.,1992), muscle injection (Ragot et al., 1993), peripheral intravenousinjections (Herz & Gerard, 1993) and stereotactic inoculation into thebrain (Le Gal La Salle et al., 1993). An example of the use of an Advector in a clinical trial involved polynucleotide therapy for antitumorimmunization with intramuscular injection (Sterman et al., Hum. GeneTher. 7:1083-9 (1998)).

In various embodiments, one or more polynucleotides encoding nucleasevariant and/or donor repair template are introduced into a hematopoieticcell by transducing the cell with a herpes simplex virus, e.g., HSV-1,HSV-2, comprising the one or more polynucleotides.

The mature HSV virion consists of an enveloped icosahedral capsid with aviral genome consisting of a linear double-stranded DNA molecule that is152 kb. In one embodiment, the HSV based viral vector is deficient inone or more essential or non-essential HSV genes. In one embodiment, theHSV based viral vector is replication deficient. Most replicationdeficient HSV vectors contain a deletion to remove one or moreintermediate-early, early, or late HSV genes to prevent replication. Forexample, the HSV vector may be deficient in an immediate early geneselected from the group consisting of: ICP4, ICP22, ICP27, ICP47, and acombination thereof. Advantages of the HSV vector are its ability toenter a latent stage that can result in long-term DNA expression and itslarge viral DNA genome that can accommodate exogenous DNA inserts of upto 25 kb. HSV-based vectors are described in, for example, U.S. Pat.Nos. 5,837,532, 5,846,782, and 5,804,413, and International PatentApplications WO 91/02788, WO 96/04394, WO 98/15637, and WO 99/06583,each of which are incorporated by reference herein in its entirety.

H. Genome Edited Cells

The genome edited cells manufactured by the methods contemplated inparticular embodiments comprise one or more gene edits in a CBLB geneand provide improved cell-based therapeutics for the prevention,treatment, or amelioration of at least one symptom, of a cancer, GVHD,infectious disease, autoimmune disease, immunodeficiency or conditionassociated therewith. Without wishing to be bound by any particulartheory, it is believed that the compositions and methods contemplatedherein increase the efficacy of adoptive cell therapies, in part, bymaking the therapeutic cells more persistent and more resistant toimmunosuppressive signals and exhaustion.

Genome edited cells contemplated in particular embodiments may beautologous/autogeneic (“self”) or non-autologous (“non-self,” e.g.,allogeneic, syngeneic or xenogeneic). “Autologous,” as used herein,refers to cells from the same subject. “Allogeneic,” as used herein,refers to cells of the same species that differ genetically to the cellin comparison. “Syngeneic,” as used herein, refers to cells of adifferent subject that are genetically identical to the cell incomparison. “Xenogeneic,” as used herein, refers to cells of a differentspecies to the cell in comparison. In preferred embodiments, the cellsare obtained from a mammalian subject. In a more preferred embodiment,the cells are obtained from a primate subject, optionally a non-humanprimate. In the most preferred embodiment, the cells are obtained from ahuman subject.

An “isolated cell” refers to a non-naturally occurring cell, e.g., acell that does not exist in nature, a modified cell, an engineered cell,etc., that has been obtained from an in vivo tissue or organ and issubstantially free of extracellular matrix.

As used herein, the term “population of cells” refers to a plurality ofcells that may be made up of any number and/or combination of homogenousor heterogeneous cell types, as described elsewhere herein. For example,for transduction of T cells, a population of cells may be isolated orobtained from peripheral blood. A population of cells may comprise about10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%,about 80%, about 90%, or about 100% of the target cell type to beedited. In certain embodiments, T cells may be isolated or purified froma population of heterogeneous cells using methods known in the art.

Illustrative examples of cell types whose genome can be edited using thecompositions and methods contemplated herein include, but are notlimited to, cell lines, primary cells, stem cells, progenitor cells, anddifferentiated cells, and mixtures thereof.

In a preferred embodiment, the genome editing compositions and methodsare used to edit hematopoietic cells, more preferably immune cells, andeven more preferably T cells.

The terms “T cell” or “T lymphocyte” are art-recognized and are intendedto include thymocytes, immune effector cells, regulatory T cells, naïveT lymphocytes, immature T lymphocytes, mature T lymphocytes, resting Tlymphocytes, or activated T lymphocytes. A T cell can be a T helper (Th)cell, for example a T helper 1 (Th1) or a T helper 2 (Th2) cell. The Tcell can be a helper T cell (HTL; CD4⁺ T cell) CD4⁺ T cell, a cytotoxicT cell (CTL; CD8⁺ T cell), a tumor infiltrating cytotoxic T cell (TIL;CD8⁺ T cell), CD4⁺CD8⁺ T cell, CD4⁻CD8⁻ T cell, or any other subset of Tcells. In one embodiment, the T cell is an immune effector cell. In oneembodiment, the T cell is an NKT cell. Other illustrative populations ofT cells suitable for use in particular embodiments include naïve T cellsand memory T cells.

In various embodiments, genome edited cells comprise immune effectorcells comprising a CBLB gene edited by the compositions and methodscontemplated herein. An “immune effector cell,” is any cell of theimmune system that has one or more effector functions (e.g., cytotoxiccell killing activity, secretion of cytokines, induction of ADCC and/orCDC). Illustrative immune effector cells contemplated in particularembodiments are T lymphocytes, in particular cytotoxic T cells (CTLs;CD8⁺ T cells), TILs, and helper T cells (HTLs; CD4⁺ T cells). In oneembodiment, immune effector cells comprise T cells. In one embodiment,immune effector cells comprise natural killer (NK) cells. In oneembodiment, immune effector cells comprise natural killer T (NKT) cells.

“Potent T cells,” and “young T cells,” are used interchangeably inparticular embodiments and refer to T cell phenotypes wherein the T cellis capable of proliferation and a concomitant decrease indifferentiation. In particular embodiments, the young T cell has thephenotype of a “naïve T cell.” In particular embodiments, young T cellscomprise one or more of, or all of the following biological markers:CD62L, CCR7, CD28, CD27, CD122, CD127, CD197, and CD38. In oneembodiment, young T cells comprise one or more of, or all of thefollowing biological markers: CD62L, CD127, CD197, and CD38. In oneembodiment, the young T cells lack expression of CD57, CD244, CD160,PD-1, CTLA4, PD-1, and LAG3.

T cells can be obtained from a number of sources including, but notlimited to, peripheral blood mononuclear cells, bone marrow, lymph nodestissue, cord blood, thymus tissue, tissue from a site of infection,ascites, pleural effusion, spleen tissue, and tumors.

In particular embodiments, a population of cells comprising immuneeffector cells or T cells comprises an edited CBLB gene, wherein theedit is a DSB repaired by NHEJ. In particular embodiments, an immuneeffector cell or T cell comprises an edited CBLB gene, wherein the editis a DSB repaired by NHEJ. In particular embodiments, the edit is aninsertion or deletion (INDEL) of about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10,11, 12, 13, 14 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25 or morenucleotides in a coding sequence of the CBLB gene, preferably in exon 6of the CBLB gene, more preferably at SEQ ID NO: 20 (or SEQ ID NO: 22) inexon 6 of the CBLB gene.

In particular embodiments, a population of cells comprising immuneeffector cells or T cells comprises an edited CBLB gene comprising adonor repair template incorporated at a DSB repaired by HDR.

In particular embodiments, a population of cells comprising immuneeffector cells or T cells comprises an edited CBLB gene comprising adonor repair template comprising a CBLB gene or portion thereof and isdesigned to introduce one or more mutations in a genomic CBLB sequenceto modify CBLB expression activity, or signaling, and preferably, todecrease or eliminate CBLB expression, activity, and/or signaling.

In various embodiments, a genome edited cell comprises an edit in theCBLB gene and further comprises a polynucleotide encoding a flipreceptor, a bispecific T cell engager (BiTE) molecule; a cytokine (e.g.,IL-2, insulin, IFN-γ, IL-7, IL-21, IL-10, IL-12, IL-15, and TNF-α), achemokine (e.g., MIP-1α, MIP-1β, MCP-1, MCP-3, and RANTES), a cytotoxin(e.g., Perform, Granzyme A, and Granzyme B), a cytokine receptor (e.g.,an IL-2 receptor, an IL-7 receptor, an IL-12 receptor, an IL-15receptor, and an IL-21 receptor), or an engineered antigen receptor(e.g., an engineered T cell receptor (TCR), a chimeric antigen receptor(CAR), a Daric receptor or components thereof, or a chimeric cytokinereceptor). In one embodiment, a donor repair template comprising thepolynucleotide and a nuclease variant are introduced into the cell andthe polynucleotide is incorporated into the cell's genome at the DSBsite in the CBLB gene by HDR repair. The polynucleotide may also beintroduced into the cell at a site other than the CBLB gene, e.g., bytransducing the cell with a vector comprising the polynucleotide.

I. Compositions and Formulations

The compositions contemplated in particular embodiments may comprise oneor more polypeptides, polynucleotides, vectors comprising same, andgenome editing compositions and genome edited cell compositions, ascontemplated herein. The genome editing compositions and methodscontemplated in particular embodiments are useful for editing a targetsite in the human CBLB gene in a cell or a population of cells. Inpreferred embodiments, a genome editing composition is used to edit aCBLB gene in a hematopoietic cell, e.g., a T cell or an immune effectorcell.

In various embodiments, the compositions contemplated herein comprise anuclease variant, and optionally an end-processing enzyme, e.g., a 3′-5′exonuclease (Trex2). The nuclease variant may be in the form of an mRNAthat is introduced into a cell via polynucleotide delivery methodsdisclosed supra, e.g., electroporation, lipid nanoparticles, etc. In oneembodiment, a composition comprising an mRNA encoding a homingendonuclease variant or megaTAL, and optionally a 3′-5′ exonuclease, isintroduced in a cell via polynucleotide delivery methods disclosedsupra. The composition may be used to generate a genome edited cell orpopulation of genome edited cells by error prone NHEJ.

In various embodiments, the compositions contemplated herein comprise adonor repair template. The composition may be delivered to a cell thatexpresses or will express nuclease variant, and optionally anend-processing enzyme. In one embodiment, the composition may bedelivered to a cell that expresses or will express a homing endonucleasevariant or megaTAL, and optionally a 3′-5′ exonuclease. Expression ofthe gene editing enzymes in the presence of the donor repair templatecan be used to generate a genome edited cell or population of genomeedited cells by HDR.

In particular embodiments, the compositions contemplated herein comprisea population of cells, a nuclease variant, and optionally, a donorrepair template. In particular embodiments, the compositionscontemplated herein comprise a population of cells, a nuclease variant,an end-processing enzyme, and optionally, a donor repair template. Thenuclease variant and/or end-processing enzyme may be in the form of anmRNA that is introduced into the cell via polynucleotide deliverymethods disclosed supra.

In particular embodiments, the compositions contemplated herein comprisea population of cells, a homing endonuclease variant or megaTAL, andoptionally, a donor repair template. In particular embodiments, thecompositions contemplated herein comprise a population of cells, ahoming endonuclease variant or megaTAL, a 3′-5′ exonuclease, andoptionally, a donor repair template. The homing endonuclease variant,megaTAL, and/or 3′-5′ exonuclease may be in the form of an mRNA that isintroduced into the cell via polynucleotide delivery methods disclosedsupra., e.g., electroporation.

In particular embodiments, the population of cells comprise geneticallymodified immune effector cells.

Compositions include, but are not limited to pharmaceuticalcompositions. A “pharmaceutical composition” refers to a compositionformulated in pharmaceutically-acceptable or physiologically-acceptablesolutions for administration to a cell or an animal, either alone, or incombination with one or more other modalities of therapy. It will alsobe understood that, if desired, the compositions may be administered incombination with other agents as well, such as, e.g., cytokines, growthfactors, hormones, small molecules, chemotherapeutics, pro-drugs, drugs,antibodies, or other various pharmaceutically-active agents. There isvirtually no limit to other components that may also be included in thecompositions, provided that the additional agents do not adverselyaffect the composition.

The phrase “pharmaceutically acceptable” is employed herein to refer tothose compounds, materials, compositions, and/or dosage forms which are,within the scope of sound medical judgment, suitable for use in contactwith the tissues of human beings and animals without excessive toxicity,irritation, allergic response, or other problem or complication,commensurate with a reasonable benefit/risk ratio.

The term “pharmaceutically acceptable carrier” refers to a diluent,adjuvant, excipient, or vehicle with which the therapeutic cells areadministered. Illustrative examples of pharmaceutical carriers can besterile liquids, such as cell culture media, water and oils, includingthose of petroleum, animal, vegetable or synthetic origin, such aspeanut oil, soybean oil, mineral oil, sesame oil and the like. Salinesolutions and aqueous dextrose and glycerol solutions can also beemployed as liquid carriers, particularly for injectable solutions.Suitable pharmaceutical excipients in particular embodiments, includestarch, glucose, lactose, sucrose, gelatin, malt, rice, flour, chalk,silica gel, sodium stearate, glycerol monostearate, talc, sodiumchloride, dried skim milk, glycerol, propylene, glycol, water, ethanoland the like. Except insofar as any conventional media or agent isincompatible with the active ingredient, its use in the therapeuticcompositions is contemplated. Supplementary active ingredients can alsobe incorporated into the compositions.

In one embodiment, a composition comprising a pharmaceuticallyacceptable carrier is suitable for administration to a subject. Inparticular embodiments, a composition comprising a carrier is suitablefor parenteral administration, e.g., intravascular (intravenous orintraarterial), intraperitoneal or intramuscular administration. Inparticular embodiments, a composition comprising a pharmaceuticallyacceptable carrier is suitable for intraventricular, intraspinal, orintrathecal administration. Pharmaceutically acceptable carriers includesterile aqueous solutions, cell culture media, or dispersions. The useof such media and agents for pharmaceutically active substances is wellknown in the art. Except insofar as any conventional media or agent isincompatible with the transduced cells, use thereof in thepharmaceutical compositions is contemplated.

In particular embodiments, compositions contemplated herein comprisegenetically modified T cells and a pharmaceutically acceptable carrier.A composition comprising a cell-based composition contemplated hereincan be administered separately by enteral or parenteral administrationmethods or in combination with other suitable compounds to effect thedesired treatment goals.

The pharmaceutically acceptable carrier must be of sufficiently highpurity and of sufficiently low toxicity to render it suitable foradministration to the human subject being treated. It further shouldmaintain or increase the stability of the composition. Thepharmaceutically acceptable carrier can be liquid or solid and isselected, with the planned manner of administration in mind, to providefor the desired bulk, consistency, etc., when combined with othercomponents of the composition. For example, the pharmaceuticallyacceptable carrier can be, without limitation, a binding agent (e.g.,pregelatinized maize starch, polyvinylpyrrolidone or hydroxypropylmethylcellulose, etc.), a filler (e.g., lactose and other sugars,microcrystalline cellulose, pectin, gelatin, calcium sulfate, ethylcellulose, polyacrylates, calcium hydrogen phosphate, etc.), a lubricant(e.g., magnesium stearate, talc, silica, colloidal silicon dioxide,stearic acid, metallic stearates, hydrogenated vegetable oils, cornstarch, polyethylene glycols, sodium benzoate, sodium acetate, etc.), adisintegrant (e.g., starch, sodium starch glycolate, etc.), or a wettingagent (e.g., sodium lauryl sulfate, etc.). Other suitablepharmaceutically acceptable carriers for the compositions contemplatedherein include, but are not limited to, water, salt solutions, alcohols,polyethylene glycols, gelatins, amyloses, magnesium stearates, talcs,silicic acids, viscous paraffins, hydroxymethylcelluloses,polyvinylpyrrolidones and the like.

Such carrier solutions also can contain buffers, diluents and othersuitable additives. The term “buffer” as used herein refers to asolution or liquid whose chemical makeup neutralizes acids or baseswithout a significant change in pH. Examples of buffers contemplatedherein include, but are not limited to, Dulbecco's phosphate bufferedsaline (PBS), Ringer's solution, 5% dextrose in water (D5W),normal/physiologic saline (0.9% NaCl).

The pharmaceutically acceptable carriers may be present in amountssufficient to maintain a pH of the composition of about 7.Alternatively, the composition has a pH in a range from about 6.8 toabout 7.4, e.g., 6.8, 6.9, 7.0, 7.1, 7.2, 7.3, and 7.4. In still anotherembodiment, the composition has a pH of about 7.4.

Compositions contemplated herein may comprise a nontoxicpharmaceutically acceptable medium. The compositions may be asuspension. The term “suspension” as used herein refers to non-adherentconditions in which cells are not attached to a solid support. Forexample, cells maintained as a suspension may be stirred or agitated andare not adhered to a support, such as a culture dish.

In particular embodiments, compositions contemplated herein areformulated in a suspension, where the genome edited T cells aredispersed within an acceptable liquid medium or solution, e.g., salineor serum-free medium, in an intravenous (IV) bag or the like. Acceptablediluents include, but are not limited to water, PlasmaLyte, Ringer'ssolution, isotonic sodium chloride (saline) solution, serum-free cellculture medium, and medium suitable for cryogenic storage, e.g.,Cryostor® medium.

In certain embodiments, a pharmaceutically acceptable carrier issubstantially free of natural proteins of human or animal origin, andsuitable for storing a composition comprising a population of genomeedited T cells. The therapeutic composition is intended to beadministered into a human patient, and thus is substantially free ofcell culture components such as bovine serum albumin, horse serum, andfetal bovine serum.

In some embodiments, compositions are formulated in a pharmaceuticallyacceptable cell culture medium. Such compositions are suitable foradministration to human subjects. In particular embodiments, thepharmaceutically acceptable cell culture medium is a serum free medium.

Serum-free medium has several advantages over serum containing medium,including a simplified and better defined composition, a reduced degreeof contaminants, elimination of a potential source of infectious agents,and lower cost. In various embodiments, the serum-free medium isanimal-free, and may optionally be protein-free. Optionally, the mediummay contain biopharmaceutically acceptable recombinant proteins.“Animal-free” medium refers to medium wherein the components are derivedfrom non-animal sources. Recombinant proteins replace native animalproteins in animal-free medium and the nutrients are obtained fromsynthetic, plant or microbial sources. “Protein-free” medium, incontrast, is defined as substantially free of protein.

Illustrative examples of serum-free media used in particularcompositions includes, but is not limited to QBSF-60 (QualityBiological, Inc.), StemPro-34 (Life Technologies), and X-VIVO 10.

In a preferred embodiment, the compositions comprising genome edited Tcells are formulated in PlasmaLyte.

In various embodiments, compositions comprising genome edited T cellsare formulated in a cryopreservation medium. For example,cryopreservation media with cryopreservation agents may be used tomaintain a high cell viability outcome post-thaw. Illustrative examplesof cryopreservation media used in particular compositions includes, butis not limited to, CryoStor CS10, CryoStor CS5, and CryoStor CS2.

In one embodiment, the compositions are formulated in a solutioncomprising 50:50 PlasmaLyte A to CryoStor CS10.

In particular embodiments, the composition is substantially free ofmycoplasma, endotoxin, and microbial contamination. By “substantiallyfree” with respect to endotoxin is meant that there is less endotoxinper dose of cells than is allowed by the FDA for a biologic, which is atotal endotoxin of 5 EU/kg body weight per day, which for an average 70kg person is 350 EU per total dose of cells. In particular embodiments,compositions comprising hematopoietic stem or progenitor cellstransduced with a retroviral vector contemplated herein contain about0.5 EU/mL to about 5.0 EU/mL, or about 0.5 EU/mL, 1.0 EU/mL, 1.5 EU/mL,2.0 EU/mL, 2.5 EU/mL, 3.0 EU/mL, 3.5 EU/mL, 4.0 EU/mL, 4.5 EU/mL, or 5.0EU/mL.

In certain embodiments, compositions and formulations suitable for thedelivery of polynucleotides are contemplated including, but not limitedto, one or more mRNAs encoding one or more reprogrammed nucleases, andoptionally end-processing enzymes.

Exemplary formulations for ex vivo delivery may also include the use ofvarious transfection agents known in the art, such as calcium phosphate,electroporation, heat shock and various liposome formulations (i.e.,lipid-mediated transfection). Liposomes, as described in greater detailbelow, are lipid bilayers entrapping a fraction of aqueous fluid. DNAspontaneously associates to the external surface of cationic liposomes(by virtue of its charge) and these liposomes will interact with thecell membrane.

In particular embodiments, formulation of pharmaceutically-acceptablecarrier solutions is well-known to those of skill in the art, as is thedevelopment of suitable dosing and treatment regimens for using theparticular compositions described herein in a variety of treatmentregimens, including e.g., enteral and parenteral, e.g., intravascular,intravenous, intrarterial, intraosseously, intraventricular,intracerebral, intracranial, intraspinal, intrathecal, andintramedullary administration and formulation. It would be understood bythe skilled artisan that particular embodiments contemplated herein maycomprise other formulations, such as those that are well known in thepharmaceutical art, and are described, for example, in Remington: TheScience and Practice of Pharmacy, volume I and volume II. 22^(nd)Edition. Edited by Loyd V. Allen Jr. Philadelphia, Pa.: PharmaceuticalPress; 2012, which is incorporated by reference herein, in its entirety.

J. Genome Edited Cell Therapies

Cells comprising an edited CBLB gene that are manufactured by thecompositions and methods contemplated herein provide improved drugproducts for use in the prevention, treatment, or amelioration of atleast one symptom of a cancer, GVHD, an infectious disease, anautoimmune disease, an inflammatory disease, or an immunodeficiency. Asused herein, the term “drug product” refers to genetically modifiedcells produced using the compositions and methods contemplated herein.In particular embodiments, the drug product comprises genetically editedimmune effector cells or T cells. In preferred embodiments, the drugproduct comprises genetically edited immune effector cells or T cellsthat express an engineered TCR or CAR or other engineered antigenreceptor. Moreover, the genome edited T cells contemplated in particularembodiments provide safer and more efficacious adoptive cell therapiesbecause they are resistant to T cell exhaustion and display increaseddurability and persistence in the tumor microenvironment that can leadto sustained therapy.

In particular embodiments, an effective amount of genome edited immuneeffector cells or T cells comprising an edited CBLB gene areadministered to a subject to prevent, treat, or ameliorate at least onesymptom of a cancer, GVHD, an infectious disease, an autoimmune disease,an inflammatory disease, or an immunodeficiency.

In particular embodiments, the CBLB edited cells do not substantiallyexpress, or lack expression of, CBLB and therefore lack or substantiallylack functional CBLB expression and/or activity, e.g., lack the abilityto increase T cell exhaustion and to inhibit expression ofproinflammatory cytokines. In particular embodiments, genome editedimmune effector cells that lack CBLB are more resistant toimmunosuppressive signals from the tumor microenvironment and displayincreased persistence and resistance to T cell exhaustion.

In particular embodiments, a method of preventing, treating, orameliorating at least one symptom of a cancer comprises administeringthe subject an effective amount of genome edited immune effector cellsor T cells comprising an edited CBLB gene and an engineered TCR, CAR, orDaric, or other therapeutic transgene to redirect the cells to a tumoror cancer. The genetically modified cells are a more durable andpersistent drug product because the cells are more resistant toimmunosuppressive signals from the tumor microenvironment by virtue ofediting the CBLB gene to decrease or eliminate CBLB expression.

In particular embodiments, genome edited cells contemplated herein areused in the treatment of solid tumors or cancers.

In particular embodiments, genome edited cells contemplated herein areused in the treatment of solid tumors or cancers including, but notlimited to: adrenal cancer, adrenocortical carcinoma, anal cancer,appendix cancer, astrocytoma, atypical teratoid/rhabdoid tumor, basalcell carcinoma, bile duct cancer, bladder cancer, bone cancer, brain/CNScancer, breast cancer, bronchial tumors, cardiac tumors, cervicalcancer, cholangiocarcinoma, chondrosarcoma, chordoma, colon cancer,colorectal cancer, craniopharyngioma, ductal carcinoma in situ (DCIS)endometrial cancer, ependymoma, esophageal cancer,esthesioneuroblastoma, Ewing's sarcoma, extracranial germ cell tumor,extragonadal germ cell tumor, eye cancer, fallopian tube cancer, fibroushistiosarcoma, fibrosarcoma, gallbladder cancer, gastric cancer,gastrointestinal carcinoid tumors, gastrointestinal stromal tumor(GIST), germ cell tumors, glioma, glioblastoma, head and neck cancer,hemangioblastoma, hepatocellular cancer, hypopharyngeal cancer,intraocular melanoma, kaposi sarcoma, kidney cancer, laryngeal cancer,leiomyosarcoma, lip cancer, liposarcoma, liver cancer, lung cancer,non-small cell lung cancer, lung carcinoid tumor, malignantmesothelioma, medullary carcinoma, medulloblastoma, menangioma,melanoma, Merkel cell carcinoma, midline tract carcinoma, mouth cancer,myxosarcoma, myelodysplastic syndrome, myeloproliferative neoplasms,nasal cavity and paranasal sinus cancer, nasopharyngeal cancer,neuroblastoma, oligodendroglioma, oral cancer, oral cavity cancer,oropharyngeal cancer, osteosarcoma, ovarian cancer, pancreatic cancer,pancreatic islet cell tumors, papillary carcinoma, paraganglioma,parathyroid cancer, penile cancer, pharyngeal cancer, pheochromocytoma,pinealoma, pituitary tumor, pleuropulmonary blastoma, primary peritonealcancer, prostate cancer, rectal cancer, retinoblastoma, renal cellcarcinoma, renal pelvis and ureter cancer, rhabdomyosarcoma, salivarygland cancer, sebaceous gland carcinoma, skin cancer, soft tissuesarcoma, squamous cell carcinoma, small cell lung cancer, smallintestine cancer, stomach cancer, sweat gland carcinoma, synovioma,testicular cancer, throat cancer, thymus cancer, thyroid cancer,urethral cancer, uterine cancer, uterine sarcoma, vaginal cancer,vascular cancer, vulvar cancer, and Wilms Tumor.

In particular embodiments, genome edited cells contemplated herein areused in the treatment of solid tumors or cancers including, withoutlimitation, liver cancer, pancreatic cancer, lung cancer, breast cancer,bladder cancer, brain cancer, bone cancer, thyroid cancer, kidneycancer, or skin cancer.

In particular embodiments, genome edited cells contemplated herein areused in the treatment of various cancers including but not limited topancreatic, bladder, and lung.

In particular embodiments, genome edited cells contemplated herein areused in the treatment of liquid cancers or hematological cancers.

In particular embodiments, genome edited cells contemplated herein areused in the treatment of B-cell malignancies, including but not limitedto: leukemias, lymphomas, and multiple myeloma.

In particular embodiments, genome edited cells contemplated herein areused in the treatment of liquid cancers including, but not limited toleukemias, lymphomas, and multiple myelomas: acute lymphocytic leukemia(ALL), acute myeloid leukemia (AML), myeloblastic, promyelocytic,myelomonocytic, monocytic, erythroleukemia, hairy cell leukemia (HCL),chronic lymphocytic leukemia (CLL), and chronic myeloid leukemia (CML),chronic myelomonocytic leukemia (CMML) and polycythemia vera, Hodgkinlymphoma, nodular lymphocyte-predominant Hodgkin lymphoma, Burkittlymphoma, small lymphocytic lymphoma (SLL), diffuse large B-celllymphoma, follicular lymphoma, immunoblastic large cell lymphoma,precursor B-lymphoblastic lymphoma, mantle cell lymphoma, marginal zonelymphoma, mycosis fungoides, anaplastic large cell lymphoma, Sézarysyndrome, precursor T-lymphoblastic lymphoma, multiple myeloma, overtmultiple myeloma, smoldering multiple myeloma, plasma cell leukemia,non-secretory myeloma, IgD myeloma, osteosclerotic myeloma, solitaryplasmacytoma of bone, and extramedullary plasmacytoma.

Preferred cells for use in the genome editing methods contemplatedherein include autologous/autogeneic (“self”) cells, preferablyhematopoietic cells, more preferably T cells, and more preferably immuneeffector cells. In one embodiment, the cells are Treg cells.

In particular embodiments, methods comprising administering atherapeutically effective amount of genome edited cells contemplatedherein or a composition comprising the same, to a patient in needthereof, alone or in combination with one or more therapeutic agents,are provided. In certain embodiments, the cells are used in thetreatment of patients at risk for developing a cancer, GVHD, aninfectious disease, an autoimmune disease, an inflammatory disease, oran immunodeficiency. Thus, particular embodiments comprise the treatmentor prevention or amelioration of at least one symptom of a cancer, aninfectious disease, an autoimmune disease, an inflammatory disease, oran immunodeficiency comprising administering to a subject in needthereof, a therapeutically effective amount of the genome edited cellscontemplated herein.

In one embodiment, a method of treating a cancer, GVHD, an infectiousdisease, an autoimmune disease, an inflammatory disease, or animmunodeficiency in a subject in need thereof comprises administering aneffective amount, e.g., therapeutically effective amount of acomposition comprising genome edited cells contemplated herein. Thequantity and frequency of administration will be determined by suchfactors as the condition of the patient, and the type and severity ofthe patient's disease, although appropriate dosages may be determined byclinical trials.

In one illustrative embodiment, the effective amount of genome editedcells provided to a subject is at least 2×10⁶ cells/kg, at least 3×10⁶cells/kg, at least 4×10⁶ cells/kg, at least 5×10⁶ cells/kg, at least6×10⁶ cells/kg, at least 7×10⁶ cells/kg, at least 8×10⁶ cells/kg, atleast 9×10⁶ cells/kg, or at least 10×10⁶ cells/kg, or more cells/kg,including all intervening doses of cells.

In another illustrative embodiment, the effective amount of genomeedited cells provided to a subject is about 2×10⁶ cells/kg, about 3×10⁶cells/kg, about 4×10⁶ cells/kg, about 5×10⁶ cells/kg, about 6×10⁶cells/kg, about 7×10⁶ cells/kg, about 8×10⁶ cells/kg, about 9×10⁶cells/kg, or about 10×10⁶ cells/kg, or more cells/kg, including allintervening doses of cells.

In another illustrative embodiment, the effective amount of genomeedited cells provided to a subject is from about 2×10⁶ cells/kg to about10×10⁶ cells/kg, about 3×10⁶ cells/kg to about 10×10⁶ cells/kg, about4×10⁶ cells/kg to about 10×10⁶ cells/kg, about 5×10⁶ cells/kg to about10×10⁶ cells/kg, 2×10⁶ cells/kg to about 6×10⁶ cells/kg, 2×10⁶ cells/kgto about 7×10⁶ cells/kg, 2×10⁶ cells/kg to about 8×10⁶ cells/kg, 3×10⁶cells/kg to about 6×10⁶ cells/kg, 3×10⁶ cells/kg to about 7×10⁶cells/kg, 3×10⁶ cells/kg to about 8×10⁶ cells/kg, 4×10⁶ cells/kg toabout 6×10⁶ cells/kg, 4×10⁶ cells/kg to about 7×10⁶ cells/kg, 4×10⁶cells/kg to about 8×10⁶ cells/kg, 5×10⁶ cells/kg to about 6×10⁶cells/kg, 5×10⁶ cells/kg to about 7×10⁶ cells/kg, 5×10⁶ cells/kg toabout 8×10⁶ cells/kg, or 6×10⁶ cells/kg to about 8×10⁶ cells/kg,including all intervening doses of cells.

One of ordinary skill in the art would recognize that multipleadministrations of the compositions contemplated in particularembodiments may be required to effect the desired therapy. For example,a composition may be administered 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 ormore times over a span of 1 week, 2 weeks, 3 weeks, 1 month, 2 months, 3months, 4 months, 5 months, 6 months, 1 year, 2 years, 5, years, 10years, or more.

In certain embodiments, it may be desirable to administer activated Tcells to a subject and then subsequently redraw blood (or have anapheresis performed), activate T cells therefrom, and reinfuse thepatient with these activated and expanded T cells. This process can becarried out multiple times every few weeks. In certain embodiments, Tcells can be activated from blood draws of from 10 cc to 400 cc. Incertain embodiments, T cells are activated from blood draws of 20 cc, 30cc, 40 cc, 50 cc, 60 cc, 70 cc, 80 cc, 90 cc, 100 cc, 150 cc, 200 cc,250 cc, 300 cc, 350 cc, or 400 cc or more. Not to be bound by theory,using this multiple blood draw/multiple reinfusion protocol may serve toselect out certain populations of T cells.

The administration of the compositions contemplated in particularembodiments may be carried out in any convenient manner, including byaerosol inhalation, injection, ingestion, transfusion, implantation ortransplantation. In a preferred embodiment, compositions areadministered parenterally. The phrases “parenteral administration” and“administered parenterally” as used herein refers to modes ofadministration other than enteral and topical administration, usually byinjection, and includes, without limitation, intravascular, intravenous,intramuscular, intraarterial, intrathecal, intracapsular, intraorbital,intratumoral, intracardiac, intradermal, intraperitoneal, transtracheal,subcutaneous, subcuticular, intraarticular, subcapsular, subarachnoid,intraspinal and intrasternal injection and infusion. In one embodiment,the compositions contemplated herein are administered to a subject bydirect injection into a tumor, lymph node, or site of infection.

In one embodiment, a method of treating a subject diagnosed with acancer, comprises removing immune effector cells from the subject,editing the genome of said immune effector cells and producing apopulation of genome edited immune effector cells, and administering thepopulation of genome edited immune effector cells to the same subject.In a preferred embodiment, the immune effector cells comprise T cells.

The methods for administering the cell compositions contemplated inparticular embodiments include any method which is effective to resultin reintroduction of ex vivo genome edited immune effector cells or onreintroduction of the genome edited progenitors of immune effector cellsthat on introduction into a subject differentiate into mature immuneeffector cells. One method comprises genome editing peripheral blood Tcells ex vivo and returning the transduced cells into the subject.

All publications, patent applications, and issued patents cited in thisspecification are herein incorporated by reference as if each individualpublication, patent application, or issued patent were specifically andindividually indicated to be incorporated by reference.

Although the foregoing embodiments have been described in some detail byway of illustration and example for purposes of clarity ofunderstanding, it will be readily apparent to one of ordinary skill inthe art in light of the teachings contemplated herein that certainchanges and modifications may be made thereto without departing from thespirit or scope of the appended claims. The following examples areprovided by way of illustration only and not by way of limitation. Thoseof skill in the art will readily recognize a variety of noncriticalparameters that could be changed or modified to yield essentiallysimilar results.

EXAMPLES Example 1 Reprogramming I-OnuI to Disrupt the Human CasitasB-Lineage (CBL) Lymphoma Proto-Oncogene B (CBLB) Gene

I-OnuI was reprogrammed to target exon 6 of the CBLB gene (FIG. 1) byconstructing modular libraries containing variable amino acid residuesin the DNA recognition interface. To construct the variants, degeneratecodons were incorporated into I-OnuI DNA binding domains usingoligonucleotides. The oligonucleotides encoding the degenerate codonswere used as PCR templates to generate variant libraries by gaprecombination in the yeast strain S. cerevisiae. Each variant libraryspanned either the N- or C-terminal I-OnuI DNA recognition domain andcontained ˜10⁷ to 10⁸ unique transformants. The resulting surfacedisplay libraries were screened by flow cytometry for cleavage activityagainst target sites comprising the corresponding domains' “half-sites”(SEQ ID NOs: 23-29), as shown in FIG. 2.

Yeast displaying the N- and C-terminal domain reprogrammed I-OnuI HEswere purified and the plasmid DNA was extracted. PCR reactions wereperformed to amplify the reprogrammed domains, which were subsequentlyfused and transformed into S. cerevisiae to create a library ofreprogrammed domain combinations. Fully reprogrammed I-OnuI variantsthat recognize the complete target site (SEQ ID NO: 20) present in exon6 of the CBLB gene were identified from this library and purified.

Example 2 Reprogrammed I-OnuI Homing Endonucleases that Target Exon 6 ofthe CBLB Gene

The activity of reprogrammed I-OnuI HEs that target exon 6 of the CBLBgene was measured using a chromosomally integrated fluorescent reportersystem (Certo et. al., 2011). Fully reprogrammed I-OnuI HEs that bindand cleave the CBLB target sequence (SEQ ID NO: 20) were cloned intomammalian expression plasmids and then individually transfected into aHEK 293T fibroblast cell line that contained the CBLB target sequenceupstream of an out-of-frame gene encoding the fluorescent iRFP protein.Cleavage of the embedded target site by the HE and the accumulation ofindels following DNA repair via the non-homologous end joining (NHEJ)pathway results in approximately one out of three repaired loci placingthe fluorescent reporter gene back “in-frame”. The percentage of iRFPfluorescing HEK 293T cells is therefore used a readout of endonucleaseactivity at the chromosomally embedded target sequence. The fullyreprogrammed I-OnuI HEs that bind and cleave the CBLB target sequenceshowed high frequency iRFP expression in a cellular chromosomal context,which indicates that the HE variants had the desired property of highediting efficiency in a cellular chromosomal context. FIG. 3.

The CBLB.E3 HE variant had sub-nanomolar affinity for the exon 6 targetsite. FIG. 4. FIG. 5 shows the relative alignments of representativeI-OnuI variants as well as the positional information of the residuescomprising the DNA recognition interface.

Example 3 Characterization of MegaTALs that Target CBLB Exon 6

The CBLB.E3, CBLB.A8, CBLB.B5, CBLB.D2, and CBLB.F6 HE variants wereformatted as megaTALs (SEQ ID NOs: 13-19) by appending an 11.5 unit TALarray, corresponding to an 12 base pair TAL array target site (SEQ IDNO: 21), to the N-terminus of the meganuclease domain (as described inBoissel et al., 2013). FIG. 6. The megaTAL target site sequence is setforth in SEQ ID NO: 22.

The megaTAL editing efficiency was assessed by pre-stimulating primaryhuman T cells with anti-CD3 and anti-CD28 antibodies incytokine-supplemented media for 48-72 hours, and then electroporatingthe cells with in vitro transcribed (IVT), capped, and polyadenylatedmRNA encoding a megaTAL. Additionally, IVT-mRNA encoding the 3′ to 5′exonuclease Trex2 was added to enhance break processing by thenon-homologous end-joining

(NHEJ) pathway (see Certo et al., 2012).

In one set of experiments, cells were cultured for 7 dayspost-electroporation (10 day total culture) and editing efficiency wasmeasured by isolating genomic DNA on days 5, 7 and 10 of culture andsequencing across the CBLB target site to measure indel frequency. FIG.7. CBLB protein levels were measured by intracellular FACS analysis ofCD3⁺ T cells. FIG. 8.

T cells or CAR T cells edited with a CBLB megaTAL showed increasedlevels of cytokine production when stimulated with anti-CD3 agonisticantibodies or CAR-specific antigen, respectively, compared to unedited Tcells and CAR T cells that either lacked active megaTAL (electroporatedwith inactive megaTAL) or lacked megaTAL altogether (no EP). FIG. 9.

In another set of experiments, cells were cultured for 7-10 days incytokine-supplemented media. At day 7 post-electoporation, genomic DNAwas isolated followed by PCR amplification across the CBLB exon 6 targetsite. The frequency of indels was measured using Tracking of Indels byDEcomposition (TIDE, see Brinkman et al., 2014). FIG. 10 shows arepresentative TIDE analysis.

Example 4 Illustrative Homology Directed Repair Strategy Using a CBLBMegatal

An adeno-associated virus (AAV) plasmid containing transgene cassettescomprising a myeloproliferative sarcoma virus enhancer, negative controlregion deleted, d1587rev primer-binding site substituted (MND) promoteroperably linked to a transgene encoding a fluorescent protein (GFP),posttranscriptional regulatory element of woodchuck hepatitis virus(WPRE) and an SV40 late polyadenylation signal was designed andconstructed (FIG. 11, AAV donor). The integrity of AAV plasmid wasconfirmed with XmaI digest and sequencing. The transgene cassette wasplaced between two 0.3 kb homology regions flanking the CBLB megaTALcleavage site (SEQ ID NO: 20, 22). Neither homology region contained thecomplete megaTAL target site.

Recombinant AAV (rAAV) was prepared by transiently co-transfecting HEK293T cells with one or more plasmids providing the replication, capsid,and adenoviral helper elements necessary. Recombinant AAV was purifiedfrom the co-transfected HEK 293T cell culture using ultracentrifugationin an iodixanol-based gradient.

megaTAL-induced homologous recombination was evaluated in primary humanT cells activated with CD3 and CD28 and cultured in complete mediasupplemented with IL-2. After 3 days, T cells were washed andelectroporated with in vitro transcribed mRNA encoding the CBLB.A8megaTAL (SEQ ID NO: 32), and subsequently transduced with purifiedrecombinant AAV encoding the DNA donor repair template comprising theMND-GFP transgene cassette described above. Flow cytometry was used atmultiple time points to measure the frequency of T cells expressing thefluorescent protein and to differentiate transient expression of thefluorescent protein from the non-integrated rAAV targeting vector.

Long-term transgene expression was observed in 21-24% of the T cellsthat were treated with both the megaTAL and the rAAV targeting vector.In contrast, untreated control samples did not express detectable levelsof fluorescent protein. Results were confirmed in experiments performedon T cells isolated from independent donors.

Example 5 CBL-B Edited Anti-EGFR CAR T Cells Show Increased Anti-TumorEfficacy in an In Vivo Tumor Model

Anti-EGFR CAR T cells were used to test the effect of CBLB gene editingon CAR T cell pharmacology in an in vivo A549 tumor model in mice.

Human PBMCs (1×10⁶ cells/mL) were activated with soluble anti-CD3 andanti-CD28 antibodies on day 0. After 24 hr incubation, 1×10⁶ cells weretransduced with an anti-EGFR CAR lentivirus. Seventy-two hourspost-antibody stimulation, transduced PBMCs or untransduced controlPBMCs were electroporated (Lonza Nucleofector) with or without in vitrotranscribed mRNA encoding a CBLB.E3 megaTAL (SEQ ID NO: 31).Electroporated cells were cultured in media containing IL-2 for 10 days.After culture, 71% of the T cells were CBLB-negative as assessed by nextgeneration sequencing (NGS) indel analysis.

Mice received a subcutaneous administration of an epithelial carcinomacell line (A549) and tumor growth was monitored using calipermeasurements. Mice were infused with equivalent CAR⁺ T cell doses (3×10⁷CAR⁺ T cells) when mean tumor volume reached 120 mm³. Vehicle treated Tcells and untransduced control T cells had minimal impact on tumorgrowth. Animals treated with anti-EGFR CAR T cells without a CBLB editwere able to delay tumor outgrowth compared to the control groups; twoof the seven mice exhibited complete tumor control. In contrast, allseven mice receiving CBLB edited anti-EGFR CAR T cells fully cleared theA549 tumors and remained tumor-free for the duration of the study (35days post CAR T cell injection).

In general, in the following claims, the terms used should not beconstrued to limit the claims to the specific embodiments disclosed inthe specification and the claims, but should be construed to include allpossible embodiments along with the full scope of equivalents to whichsuch claims are entitled. Accordingly, the claims are not limited by thedisclosure.

1.-138. (canceled)
 139. A polynucleotide encoding a fusion polypeptidecomprising an amino acid sequence at least 95% identical to the aminoacid sequence set forth in SEQ ID NO: 13, wherein the polypeptide bindsto and cleaves a target site in a human Cbl lymphoma proto-oncogene B(CBLB) gene set forth in SEQ ID NO:
 22. 140. The polynucleotide of claim139, wherein the fusion polypeptide comprises an amino acid sequence atleast 99% identical to the amino acid sequence set forth in SEQ ID NO:13.
 141. The polynucleotide of claim 139, wherein the fusion polypeptidecomprises the amino acid sequence set forth in SEQ ID NO:
 13. 142. Thepolynucleotide of claim 139, wherein the fusion polypeptide comprisesthe amino acid sequence set forth in SEQ ID NO:
 14. 143. Thepolynucleotide of claim 139, wherein the fusion polypeptide comprisesthe amino acid sequence set forth in SEQ ID NO:
 15. 144. Thepolynucleotide of claim 139, wherein the fusion polypeptide comprisesthe amino acid sequence set forth in SEQ ID NO:
 16. 145. Thepolynucleotide of claim 139, wherein the fusion polypeptide comprisesthe amino acid sequence set forth in SEQ ID NO:
 17. 146. Thepolynucleotide of claim 139, wherein the fusion polypeptide comprisesthe amino acid sequence set forth in SEQ ID NO:
 18. 147. Thepolynucleotide of claim 139, wherein the fusion polypeptide comprisesthe amino acid sequence set forth in SEQ ID NO:
 19. 148. Thepolynucleotide of claim 139, wherein the polynucleotide is a cDNA. 149.The polynucleotide of claim 139, wherein the polynucleotide is an mRNA.150. The polynucleotide of claim 139, wherein the polynucleotidecomprises the sequence set forth in SEQ ID NO: 31.